FDA 510(k)

YERSINIA AGAR BASE & SUPPLEMENT

K-Number: K822659 · 1982-09-21

Decision Date1982-09-21

Product CodeJSJ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

YERSINIA AGAR BASE & SUPPLEMENT 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 K822659. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YERSINIA AGAR BASE & SUPPLEMENT?

YERSINIA AGAR BASE & SUPPLEMENT 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 K822659.

When did YERSINIA AGAR BASE & SUPPLEMENT receive FDA 510(k) clearance?

YERSINIA AGAR BASE & SUPPLEMENT received FDA 510(k) clearance on 1982-09-21, under 510(k) number K822659.

Who is the listed applicant for YERSINIA AGAR BASE & SUPPLEMENT?

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 YERSINIA AGAR BASE & SUPPLEMENT?

The FDA product code for YERSINIA AGAR BASE & SUPPLEMENT is JSJ.

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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.