FDA 510(k)

URI-DRAIN COMBO KIT FOR MALE INCONTINENC

K-Number: K770789 · 1977-10-18

Decision Date1977-10-18

Product CodeKNX

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

URI-DRAIN COMBO KIT FOR MALE INCONTINENC is the device name listed in this FDA 510(k) record. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. It received FDA 510(k) clearance on 1977-10-18 under 510(k) number K770789. The device is classified under product code KNX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URI-DRAIN COMBO KIT FOR MALE INCONTINENC?

URI-DRAIN COMBO KIT FOR MALE INCONTINENC is a medical device that received FDA 510(k) clearance on 1977-10-18. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K770789.

When did URI-DRAIN COMBO KIT FOR MALE INCONTINENC receive FDA 510(k) clearance?

URI-DRAIN COMBO KIT FOR MALE INCONTINENC received FDA 510(k) clearance on 1977-10-18, under 510(k) number K770789.

Who is the listed applicant for URI-DRAIN COMBO KIT FOR MALE INCONTINENC?

The FDA 510(k) record lists Chesebrough-Pond'S U.S.A. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URI-DRAIN COMBO KIT FOR MALE INCONTINENC?

The FDA product code for URI-DRAIN COMBO KIT FOR MALE INCONTINENC is KNX.

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Related Devices (Code: KNX)

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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.