Visera Hysterovideoscope Olympus Hyf Type V

FDA 510(k) K022445 · Olympus Optical Co., Ltd.

Substantially Equivalent

510(k) numberK022445

Submission

Device name
Visera Hysterovideoscope Olympus Hyf Type V
Applicant
Olympus Optical Co., Ltd.
Melville, NY, US
Received
July 25, 2002
Decision date
January 24, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HIH – Hysteroscope (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 884.1690
Specialty
Obstetrics/Gynecology

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Questions and answers

When was Visera Hysterovideoscope Olympus Hyf Type V cleared by the FDA?

Visera Hysterovideoscope Olympus Hyf Type V (K022445) received a 510(k) decision of Substantially Equivalent on January 24, 2003, 183 days after the submission was received.

What is the product code of K022445?

The FDA product code is HIH – Hysteroscope (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 884.1690.