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FDA 510(k)

ANGLED TIP POLYPECTOMY SNARE

K-Number: K970945 · 1997-05-07

ApplicantUnited States Endoscopy Group, Inc.
Decision Date1997-05-07
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ANGLED TIP POLYPECTOMY SNARE 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 1997-05-07 under 510(k) number K970945. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGLED TIP POLYPECTOMY SNARE?

ANGLED TIP POLYPECTOMY SNARE is a medical device that received FDA 510(k) clearance on 1997-05-07. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K970945.

When did ANGLED TIP POLYPECTOMY SNARE receive FDA 510(k) clearance?

ANGLED TIP POLYPECTOMY SNARE received FDA 510(k) clearance on 1997-05-07, under 510(k) number K970945.

Who is the listed applicant for ANGLED TIP POLYPECTOMY SNARE?

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 ANGLED TIP POLYPECTOMY SNARE?

The FDA product code for ANGLED TIP POLYPECTOMY SNARE is KNS.

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Related Devices (Code: KNS)

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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