Omegascope

FDA 510(k) K924228 · Omega Universal Technologies, Ltd.

Substantially Equivalent

510(k) numberK924228

Submission

Device name
Omegascope
Applicant
Omega Universal Technologies, Ltd.
Marlboro, NJ, US
Received
August 21, 1992
Decision date
February 26, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

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

to examine and perform procedures within the bile ducts. 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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K231105Flexible Choledochoscope (Model: CS50H-20EU, CS50H-20US)FBN · Traditional Shanghai AnQing Medical Instrument Co., Ltd.10/17/2023SE
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More from Zhuhai Pusen Medical Technology Co., Ltd.

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K920439Omega Oto Nasopharyngo-LaryngoscopeEOB · Traditional 09/04/1992SE
K911090Omega Angioscopes (Omegascopes)LYK · Traditional 07/31/1991SE

Questions and answers

When was Omegascope cleared by the FDA?

Omegascope (K924228) received a 510(k) decision of Substantially Equivalent on February 26, 1993, 189 days after the submission was received.

What is the product code of K924228?

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