PENTAX Medical Video Duodenoscope (ED34-i10T2s); PENTAX Medical Video Processor (EPK-i8020c); PENTAX Medical Single Use, Sterile Distal End Cap with Elevator (OE-A63); Gas/Water Feeding Valves (OF-B194 )

FDA 510(k) K233942 · Pentax of America, Inc.

Substantially Equivalent

510(k) numberK233942

Submission

Device name
PENTAX Medical Video Duodenoscope (ED34-i10T2s); PENTAX Medical Video Processor (EPK-i8020c); PENTAX Medical Single Use, Sterile Distal End Cap with Elevator (OE-A63); Gas/Water Feeding Valves (OF-B194 )
Applicant
Pentax of America, Inc.
Montvale, NJ, US
Received
December 14, 2023
Decision date
August 1, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FDT – Duodenoscope And Accessories, Flexible/Rigid
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

To examine the duodenum and to perform various procedures within the duodenum. If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

Other 510(k)s with product code FDT

510(k)DeviceApplicantDecision
K251861FUJIFILM Endoscope Model ED-S100TP; FUJIFILM Endoscope Model ED-S100XP; FUJIFILM…FDT · Traditional Fujifilm Corporation03/09/2026SE
K253646Single Use Distal Cover MAJ-2315 (MAJ-2315)FDT · Traditional Olympus Medical Systems Corp.02/22/2026SE
K251867Evis Exera III Duodenovideoscope Olympus TJF-Q190V (TJF-Q190V)FDT · Traditional Olympus Medical Systems Corp.09/19/2025SE
K250701Evis Exera III Duodenovideoscope Olympus TJF-Q190V (TJF-Q190V)FDT · Traditional Olympus Medical Systems Corp.06/05/2025SE
K233886Ambu® aScope™ Duodeno 2, Ambu® aBox™ 2FDT · Traditional Ambu A/S04/16/2024SE
K220587Evis Exera III Duodenovideoscope Olympus TJF-Q190VFDT · Traditional Olympus Medical Systems Corp.05/11/2022SE
K210710PENTAX Medical Video Duedenoscope ED34-i10T2FDT · Special Pentax of America, Inc.04/09/2021SE
K202365Pentax Medical Video Duodenoscope ED32-i10FDT · Traditional Pentax of America, Inc.04/01/2021SE
K202661Evis Exera III Duodenovideoscope Olympus TJF-Q190VFDT · Traditional Olympus Medical Systems Corp.12/08/2020SE
K203028FUJIFILM Distal End CapFDT · Special Fujifilm Corporation10/30/2020SE

More from Fujifilm Corporation

510(k)DeviceDecision
K251256PENTAX Medical Video Upper GI Scopes (EG Family) (EG Family); PENTAX Medical Video…FDS · Traditional 12/16/2025SE
K251127PENTAX Medical Video Processor (EPK-i8020c)PEA · Traditional 06/03/2025SE
K242110PENTAX Medical Video Colonoscope (EC38-i20cWL)FDF · Traditional 01/03/2025SE
K241213PENTAX Medical Video Upper GI Scope (EG27-i20c); PENTAX Medical Video Colonoscope…FDS · Traditional 12/06/2024SE
K240457C2 CryoBalloon Ablation System (C2 CryoBalloon Ablation System)GEH · Traditional 07/24/2024SE
K232860PENTAX Medical Video Processor EPK-i8020c, PENTAX Medical Video Bronchoscope EB11-J10…EOQ · Traditional 01/18/2024SE
K231970PENTAX Medical Single Use Video Bronchoscope EB11-S01, PENTAX Medical Single Use Video…EOQ · Traditional 01/12/2024SE
K232249PENTAX Medical Gas/Water Feeding Valve OE-B14ODC · Traditional 12/01/2023SE
K231249PENTAX Medical Video Processor EPK-i8020c, PENTAX Medical Video Upper GI Scope…PEA · Traditional 07/28/2023SE
K213235PENTAX Medical ONE Pulmo Single Use Video Bronchoscope SystemEOQ · Traditional 12/21/2022SE

Questions and answers

When was PENTAX Medical Video Duodenoscope (ED34-i10T2s); PENTAX Medical Video Processor (EPK-i8020c); PENTAX Medical Single Use, Sterile Distal End Cap with Elevator (OE-A63); Gas/Water Feeding Valves (OF-B194 ) cleared by the FDA?

PENTAX Medical Video Duodenoscope (ED34-i10T2s); PENTAX Medical Video Processor (EPK-i8020c); PENTAX Medical Single Use, Sterile Distal End Cap with Elevator (OE-A63); Gas/Water Feeding Valves (OF-B194 ) (K233942) received a 510(k) decision of Substantially Equivalent on August 1, 2024, 231 days after the submission was received.

What is the product code of K233942?

The FDA product code is FDT – Duodenoscope And Accessories, Flexible/Rigid, a Class II (moderate risk) device regulated under 21 CFR 876.1500.