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FDA 510(k)

ENDOSNARE

K-Number: K923031 · 1993-06-07

ApplicantCook Urological, Inc.
Decision Date1993-06-07
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSNARE is the device name listed in this FDA 510(k) record. The listed applicant is Cook Urological, Inc.. It received FDA 510(k) clearance on 1993-06-07 under 510(k) number K923031. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSNARE?

ENDOSNARE is a medical device that received FDA 510(k) clearance on 1993-06-07. The listed applicant is Cook Urological, Inc.. The 510(k) number is K923031.

When did ENDOSNARE receive FDA 510(k) clearance?

ENDOSNARE received FDA 510(k) clearance on 1993-06-07, under 510(k) number K923031.

Who is the listed applicant for ENDOSNARE?

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

What is the FDA product code for ENDOSNARE?

The FDA product code for ENDOSNARE is FDI.

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Other records listing Cook Urological, Inc. as applicant

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Related Devices (Code: FDI)

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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