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FDA 510(k)

CARAFE, PERSONAL, 1-QT SEMI-RECTANGULAR

K-Number: K760072 · 1976-07-20

ApplicantBemis Health Care
Decision Date1976-07-20
Product Code
DecisionSubstantially Equivalent

Device Summary

CARAFE, PERSONAL, 1-QT SEMI-RECTANGULAR 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 1976-07-20 under 510(k) number K760072. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARAFE, PERSONAL, 1-QT SEMI-RECTANGULAR?

CARAFE, PERSONAL, 1-QT SEMI-RECTANGULAR is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Bemis Health Care. The 510(k) number is K760072.

When did CARAFE, PERSONAL, 1-QT SEMI-RECTANGULAR receive FDA 510(k) clearance?

CARAFE, PERSONAL, 1-QT SEMI-RECTANGULAR received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760072.

Who is the listed applicant for CARAFE, PERSONAL, 1-QT SEMI-RECTANGULAR?

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

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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 CANISTERK771738MALE URINAL

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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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