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FDA 510(k)

STRYKER VISION ELECT WHDTV (STRYKER VE WHDTV)

K-Number: K081995 · 2008-10-02

ApplicantStryker Endoscopy
Decision Date2008-10-02
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STRYKER VISION ELECT WHDTV (STRYKER VE WHDTV) is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 2008-10-02 under 510(k) number K081995. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER VISION ELECT WHDTV (STRYKER VE WHDTV)?

STRYKER VISION ELECT WHDTV (STRYKER VE WHDTV) is a medical device that received FDA 510(k) clearance on 2008-10-02. The listed applicant is Stryker Endoscopy. The 510(k) number is K081995.

When did STRYKER VISION ELECT WHDTV (STRYKER VE WHDTV) receive FDA 510(k) clearance?

STRYKER VISION ELECT WHDTV (STRYKER VE WHDTV) received FDA 510(k) clearance on 2008-10-02, under 510(k) number K081995.

Who is the listed applicant for STRYKER VISION ELECT WHDTV (STRYKER VE WHDTV)?

The FDA 510(k) record lists Stryker Endoscopy as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRYKER VISION ELECT WHDTV (STRYKER VE WHDTV)?

The FDA product code for STRYKER VISION ELECT WHDTV (STRYKER VE WHDTV) is GCJ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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