Visera Cystovideoscope Olympus Cyf Type V/Va

FDA 510(k) K021074 · Olympus America, Inc.

Substantially Equivalent

510(k) numberK021074

Submission

Device name
Visera Cystovideoscope Olympus Cyf Type V/Va
Applicant
Olympus America, Inc.
Melville, NY, US
Received
April 2, 2002
Decision date
May 2, 2002
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FAJ – Cystoscope 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 urinary tract. 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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Questions and answers

When was Visera Cystovideoscope Olympus Cyf Type V/Va cleared by the FDA?

Visera Cystovideoscope Olympus Cyf Type V/Va (K021074) received a 510(k) decision of Substantially Equivalent on May 2, 2002, 30 days after the submission was received.

What is the product code of K021074?

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