FDA 510(k)

WILKINS-CHALGREN ANAEROBE BROTH

K-Number: K822665 · 1982-09-21

Decision Date1982-09-21

Product CodeJSC

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

WILKINS-CHALGREN ANAEROBE BROTH is the device name listed in this FDA 510(k) record. The listed applicant is Oxoid U.S.A., Inc.. It received FDA 510(k) clearance on 1982-09-21 under 510(k) number K822665. The device is classified under product code JSC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILKINS-CHALGREN ANAEROBE BROTH?

WILKINS-CHALGREN ANAEROBE BROTH is a medical device that received FDA 510(k) clearance on 1982-09-21. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K822665.

When did WILKINS-CHALGREN ANAEROBE BROTH receive FDA 510(k) clearance?

WILKINS-CHALGREN ANAEROBE BROTH received FDA 510(k) clearance on 1982-09-21, under 510(k) number K822665.

Who is the listed applicant for WILKINS-CHALGREN ANAEROBE BROTH?

The FDA 510(k) record lists Oxoid U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WILKINS-CHALGREN ANAEROBE BROTH?

The FDA product code for WILKINS-CHALGREN ANAEROBE BROTH is JSC.

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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.