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FDA 510(k)

STRYKER ENDOSCOPIC VIDEO ACCESSORIES

K-Number: K935234 · 1994-03-18

ApplicantStryker Endoscopy
Decision Date1994-03-18
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STRYKER ENDOSCOPIC VIDEO ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 1994-03-18 under 510(k) number K935234. 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 ENDOSCOPIC VIDEO ACCESSORIES?

STRYKER ENDOSCOPIC VIDEO ACCESSORIES is a medical device that received FDA 510(k) clearance on 1994-03-18. The listed applicant is Stryker Endoscopy. The 510(k) number is K935234.

When did STRYKER ENDOSCOPIC VIDEO ACCESSORIES receive FDA 510(k) clearance?

STRYKER ENDOSCOPIC VIDEO ACCESSORIES received FDA 510(k) clearance on 1994-03-18, under 510(k) number K935234.

Who is the listed applicant for STRYKER ENDOSCOPIC VIDEO ACCESSORIES?

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 ENDOSCOPIC VIDEO ACCESSORIES?

The FDA product code for STRYKER ENDOSCOPIC VIDEO ACCESSORIES is GCJ.

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Related Devices (Code: GCJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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