FDA 510(k)

STRYKER ENDOSCOPIC ELECTROSURGICAL INSTRUMENTS & ACCESORIES

K-Number: K935222 · 1994-03-25

Decision Date1994-03-25

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

STRYKER ENDOSCOPIC ELECTROSURGICAL INSTRUMENTS & ACCESORIES is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 1994-03-25 under 510(k) number K935222. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER ENDOSCOPIC ELECTROSURGICAL INSTRUMENTS & ACCESORIES?

STRYKER ENDOSCOPIC ELECTROSURGICAL INSTRUMENTS & ACCESORIES is a medical device that received FDA 510(k) clearance on 1994-03-25. The listed applicant is Stryker Endoscopy. The 510(k) number is K935222.

When did STRYKER ENDOSCOPIC ELECTROSURGICAL INSTRUMENTS & ACCESORIES receive FDA 510(k) clearance?

STRYKER ENDOSCOPIC ELECTROSURGICAL INSTRUMENTS & ACCESORIES received FDA 510(k) clearance on 1994-03-25, under 510(k) number K935222.

Who is the listed applicant for STRYKER ENDOSCOPIC ELECTROSURGICAL INSTRUMENTS & ACCESORIES?

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 ELECTROSURGICAL INSTRUMENTS & ACCESORIES?

The FDA product code for STRYKER ENDOSCOPIC ELECTROSURGICAL INSTRUMENTS & ACCESORIES is GEI.

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Official Source

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