Evis Exera III Colonovideoscope Olympus PCF-H190TL, Evis Exera III Colonovideoscope Olympus PCF-H190TI, Evis Exera III Colonovideoscope Olympus PCF-HQ190L, Evis Exera III Colonovideoscope Olympus PCF-HQ190I

FDA 510(k) K192793 · Olympus Medical Systems Corp.

Substantially Equivalent

510(k) numberK192793

Submission

Device name
Evis Exera III Colonovideoscope Olympus PCF-H190TL, Evis Exera III Colonovideoscope Olympus PCF-H190TI, Evis Exera III Colonovideoscope Olympus PCF-HQ190L, Evis Exera III Colonovideoscope Olympus PCF-HQ190I
Applicant
Olympus Medical Systems Corp.
Hachioji-Shi, JP
Received
September 30, 2019
Decision date
July 17, 2020
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

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

To examine or perform procedures in the colon or rectum For reusable, flexible endoscopes in this product code, validated reprocessing instructions and reprocessing validation data 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).

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K260503Triton 1 SystemFDF · Traditional Neptune Medical, Inc.09/03/2026SE
K261015Solo Scope Colonoscope SystemFDF · Traditional Gi View, Ltd.08/21/2026SE
K261587Insufflation Retention Device (IRD) (11173-325-101)FDF · Special BPEndo, LLC07/02/2026SE
K260423Disposable Endoscopic Distal AttachmentsFDF · Traditional Yangzhou Fartley Medical Instrument Technology…05/28/2026SE
K252457Disposable Distal End Tape HoodFDF · Traditional Shanghai SeeGen Photoelectric Technology Co., Ltd.01/30/2026SE
K244029Robopera (ER-R-002); Robopera (ER-R-003)FDF · Traditional Endorobotics Co., Ltd.09/24/2025SE
K243261FUJIFILM Endoscope Model EC-860P/M; FUJIFILM Endoscope Model EC-860P/L; FUJIFILM…FDF · Traditional Fujifilm Corporation05/23/2025SE
K250432Colonovideoscope (CF-EZ1500DL); Colonovideoscope (CF-EZ1500DI); Gastrointestinal…FDF · Traditional Olympus Medical Systems Corporation05/15/2025SE
K242110PENTAX Medical Video Colonoscope (EC38-i20cWL)FDF · Traditional Pentax of America, Inc.01/03/2025SE
K242325GripTract-GI Endoscopic Tissue Manipulator Lower GI ModelsFDF · Traditional Actuated Medical, Inc.10/04/2024SE

More from Actuated Medical, Inc.

510(k)DeviceDecision
K2620794K Camera Head OLYMPUS CH-S700-08-LBFET · Traditional 09/10/2026SE
K260856Disposable Distal Attachment D-201-13404FDS · Traditional 08/27/2026SE
K260824Gastrointestinal Videoscope Olympus GIF-2T1500FDS · Traditional 08/27/2026SE
K260401Evis Eus Ultrasound Bronchofibervideoscope Olympus BF-UCP190F (BF-UCP190F)PSV · Traditional 08/27/2026SE
K261183EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)ODG · Traditional 07/31/2026SE
K254056THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip Type S (TB-0545FCS); THUNDERBEAT 5 mm, 35…GEI · Traditional 07/01/2026SE
K261260HD Camera Head OLYMPUS CH-S200-08-LBFET · Traditional 06/24/2026SE
K260580Single Use Reloadable Clip Applicator (HX-810LR, HX-810UR); Clip (HX-610-090…PKL · Traditional 05/21/2026SE
K252341Evis Exera III Bronchovideoscope (Olympus BF-Q190); Evis Exera III Bronchovideoscope…EOQ · Traditional 04/23/2026SE
K252050Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241DEOB · Traditional 03/20/2026SE

Questions and answers

When was Evis Exera III Colonovideoscope Olympus PCF-H190TL, Evis Exera III Colonovideoscope Olympus PCF-H190TI, Evis Exera III Colonovideoscope Olympus PCF-HQ190L, Evis Exera III Colonovideoscope Olympus PCF-HQ190I cleared by the FDA?

Evis Exera III Colonovideoscope Olympus PCF-H190TL, Evis Exera III Colonovideoscope Olympus PCF-H190TI, Evis Exera III Colonovideoscope Olympus PCF-HQ190L, Evis Exera III Colonovideoscope Olympus PCF-HQ190I (K192793) received a 510(k) decision of Substantially Equivalent on July 17, 2020, 291 days after the submission was received.

What is the product code of K192793?

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