Olympus MH-246R Balloon Sheath, for Bronchial Use

FDA 510(k) K982733 · The Olympus Optical Co.

Substantially Equivalent

510(k) numberK982733

Submission

Device name
Olympus MH-246R Balloon Sheath, for Bronchial Use
Applicant
The Olympus Optical Co.
Melville, NY, US
Received
August 5, 1998
Decision date
October 28, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
ITX – Transducer, Ultrasonic, Diagnostic
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1570
Specialty
Radiology

Other 510(k)s with product code ITX

510(k)DeviceApplicantDecision
K261170BA-004CCITX · Traditional Fujifilm Corporation08/12/2026SE
K254143EM-TECH Passive Ultrasound Probe StrapITX · Traditional EM-TECH Solutions, Inc.08/10/2026SE
K260161SmartGuide Disposable Guides and GridsITX · Traditional UC-CARE , Ltd.07/30/2026SE
K262474ND Needle Guidance SystemITX · Traditional Accurate Access, LLC07/27/2026SE
K261014Accuro® 3S Needle Guide KitITX · Traditional Rivanna Medical, Inc.07/24/2026SE
K250883Ultrasonic Probe UM-3R (UM-3R); Ultrasonic Probe UM-G20-29R (UM-G20-29R)ITX · Traditional Olympus Medical Systems Corporation09/18/2025SE
K250762Ultrasonic Probe UM-S20-17S (UM-S20-17S); Ultrasonic Probe UM-S20-20R (UM-S20-20R)ITX · Traditional Olympus Medical Systems Corporation07/11/2025SE
K250524Mendaera Guidance SystemITX · Traditional Mendaera, Inc.07/02/2025SE
K250469Accuro® 3S Needle Guide KitITX · Traditional Rivanna Medical, Inc.06/13/2025SE
K241662Ultrasound Transducer CoverITX · Traditional Vitrolife Sweden AB08/30/2024SE

More from Vitrolife Sweden AB

510(k)DeviceDecision
K033225Evis Exera Bronchofibervideoscope Olympus BF Type XP160F, Its Accessories and Ancillary…EOQ · Traditional 10/16/2003SE
K032066Sonosurg SystemLFL · Traditional 10/03/2003SE
K031305Olympus Ultrasonic Surgical SystemLFL · Traditional 09/23/2003SE
K031648Visera Rhino-Laryngovideoscope Olympus Enf Type VEOB · Traditional 07/24/2003SE
K032092Olympus XCYF-TP3 Cystofiberscope/NephrofiberscopeFCL · Traditional 07/16/2003SE
K031347Ultrasonic Gastrovideoscope, Type UC160P-AT8 and UCT160-AT8ODG · Traditional 05/09/2003SE
K030194XUES-41 Endoscopic Electrosurgical UnitKNS · Traditional 03/24/2003SE
K024138Heat Scissors Generator Set and Heat Scissors HandpieceGEI · Traditional 03/12/2003SE
K021962Olympus Ultrasonic Surgical SystemLFL · Traditional 02/12/2003SE
K021852Olympus PSD-20 Electrosurgical System & Its Associated AccessoriesGEI · Traditional 02/11/2003SE

Questions and answers

When was Olympus MH-246R Balloon Sheath, for Bronchial Use cleared by the FDA?

Olympus MH-246R Balloon Sheath, for Bronchial Use (K982733) received a 510(k) decision of Substantially Equivalent on October 28, 1998, 84 days after the submission was received.

What is the product code of K982733?

The FDA product code is ITX – Transducer, Ultrasonic, Diagnostic, a Class II (moderate risk) device regulated under 21 CFR 892.1570.