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FDA 510(k)

COOK COAGULATOR PROBE

K-Number: K935874 · 1994-03-07

ApplicantCook Urological, Inc.
Decision Date1994-03-07
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COOK COAGULATOR PROBE 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 1994-03-07 under 510(k) number K935874. 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 COOK COAGULATOR PROBE?

COOK COAGULATOR PROBE is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Cook Urological, Inc.. The 510(k) number is K935874.

When did COOK COAGULATOR PROBE receive FDA 510(k) clearance?

COOK COAGULATOR PROBE received FDA 510(k) clearance on 1994-03-07, under 510(k) number K935874.

Who is the listed applicant for COOK COAGULATOR PROBE?

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 COOK COAGULATOR PROBE?

The FDA product code for COOK COAGULATOR PROBE is GEI.

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Other records listing Cook Urological, Inc. as applicant

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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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