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FDA 510(k)

POLYP SNARE NET W/MONOPOLAR CAUTERY

K-Number: K926103 · 1993-09-23

Decision Date1993-09-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

POLYP SNARE NET W/MONOPOLAR CAUTERY is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 1993-09-23 under 510(k) number K926103. 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 POLYP SNARE NET W/MONOPOLAR CAUTERY?

POLYP SNARE NET W/MONOPOLAR CAUTERY is a medical device that received FDA 510(k) clearance on 1993-09-23. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K926103.

When did POLYP SNARE NET W/MONOPOLAR CAUTERY receive FDA 510(k) clearance?

POLYP SNARE NET W/MONOPOLAR CAUTERY received FDA 510(k) clearance on 1993-09-23, under 510(k) number K926103.

Who is the listed applicant for POLYP SNARE NET W/MONOPOLAR CAUTERY?

The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POLYP SNARE NET W/MONOPOLAR CAUTERY?

The FDA product code for POLYP SNARE NET W/MONOPOLAR CAUTERY is GEI.

Related Clinical Trials

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.

Other records listing United States Endoscopy Group, Inc. as applicant

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.

View all 85 devices →

Related Devices (Code: GEI)

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.

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.

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