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FDA 510(k)

FEATHER-LITE URINARY DIV. POUCH

K-Number: K792139 · 1979-11-13

ApplicantHowmedica Corp.
Decision Date1979-11-13
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FEATHER-LITE URINARY DIV. POUCH is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1979-11-13 under 510(k) number K792139. The device is classified under product code EXB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEATHER-LITE URINARY DIV. POUCH?

FEATHER-LITE URINARY DIV. POUCH is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Howmedica Corp.. The 510(k) number is K792139.

When did FEATHER-LITE URINARY DIV. POUCH receive FDA 510(k) clearance?

FEATHER-LITE URINARY DIV. POUCH received FDA 510(k) clearance on 1979-11-13, under 510(k) number K792139.

Who is the listed applicant for FEATHER-LITE URINARY DIV. POUCH?

The FDA 510(k) record lists Howmedica Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FEATHER-LITE URINARY DIV. POUCH?

The FDA product code for FEATHER-LITE URINARY DIV. POUCH is EXB.

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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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