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FDA 510(k)

MALE URINAL

K-Number: K771738 · 1977-09-28

ApplicantBemis Health Care
Decision Date1977-09-28
Product CodeFNP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MALE URINAL is the device name listed in this FDA 510(k) record. The listed applicant is Bemis Health Care. It received FDA 510(k) clearance on 1977-09-28 under 510(k) number K771738. The device is classified under product code FNP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MALE URINAL?

MALE URINAL is a medical device that received FDA 510(k) clearance on 1977-09-28. The listed applicant is Bemis Health Care. The 510(k) number is K771738.

When did MALE URINAL receive FDA 510(k) clearance?

MALE URINAL received FDA 510(k) clearance on 1977-09-28, under 510(k) number K771738.

Who is the listed applicant for MALE URINAL?

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

What is the FDA product code for MALE URINAL?

The FDA product code for MALE URINAL is FNP.

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Other records listing Bemis Health Care as applicant

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.

K885019BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI.K822557SPECIMEN ADAPTORK822556CRITICAL MEASUREMENT UNITK803206SUCTION PROBEK771737SUCTION CANISTERK7717338 EMESIS BASIN

View all 12 devices →

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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