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FDA 510(k)

WILLIAMS PENILE ANESTHETIC RETAINER

K-Number: K896160 · 1990-02-16

ApplicantCook Urological, Inc.
Decision Date1990-02-16
Product CodeFHA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WILLIAMS PENILE ANESTHETIC RETAINER 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 1990-02-16 under 510(k) number K896160. The device is classified under product code FHA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILLIAMS PENILE ANESTHETIC RETAINER?

WILLIAMS PENILE ANESTHETIC RETAINER is a medical device that received FDA 510(k) clearance on 1990-02-16. The listed applicant is Cook Urological, Inc.. The 510(k) number is K896160.

When did WILLIAMS PENILE ANESTHETIC RETAINER receive FDA 510(k) clearance?

WILLIAMS PENILE ANESTHETIC RETAINER received FDA 510(k) clearance on 1990-02-16, under 510(k) number K896160.

Who is the listed applicant for WILLIAMS PENILE ANESTHETIC RETAINER?

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 WILLIAMS PENILE ANESTHETIC RETAINER?

The FDA product code for WILLIAMS PENILE ANESTHETIC RETAINER is FHA.

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Related Devices (Code: FHA)

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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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