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FDA 510(k)

QUESTUS DISPOSABLE ENDOSCOPIC KNIFE

K-Number: K952926 · 1995-07-31

ApplicantWrightmedicaltechnologyinc
Decision Date1995-07-31
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

QUESTUS DISPOSABLE ENDOSCOPIC KNIFE is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1995-07-31 under 510(k) number K952926. 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 QUESTUS DISPOSABLE ENDOSCOPIC KNIFE?

QUESTUS DISPOSABLE ENDOSCOPIC KNIFE is a medical device that received FDA 510(k) clearance on 1995-07-31. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K952926.

When did QUESTUS DISPOSABLE ENDOSCOPIC KNIFE receive FDA 510(k) clearance?

QUESTUS DISPOSABLE ENDOSCOPIC KNIFE received FDA 510(k) clearance on 1995-07-31, under 510(k) number K952926.

Who is the listed applicant for QUESTUS DISPOSABLE ENDOSCOPIC KNIFE?

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

What is the FDA product code for QUESTUS DISPOSABLE ENDOSCOPIC KNIFE?

The FDA product code for QUESTUS DISPOSABLE ENDOSCOPIC KNIFE 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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