FDA 510(k)

MYCOPLASMA SUPPLEMENT G

K-Number: K800253 · 1980-03-12

Decision Date1980-03-12

Product CodeJSK

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

MYCOPLASMA SUPPLEMENT G 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 1980-03-12 under 510(k) number K800253. The device is classified under product code JSK. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYCOPLASMA SUPPLEMENT G?

MYCOPLASMA SUPPLEMENT G is a medical device that received FDA 510(k) clearance on 1980-03-12. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K800253.

When did MYCOPLASMA SUPPLEMENT G receive FDA 510(k) clearance?

MYCOPLASMA SUPPLEMENT G received FDA 510(k) clearance on 1980-03-12, under 510(k) number K800253.

Who is the listed applicant for MYCOPLASMA SUPPLEMENT G?

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 MYCOPLASMA SUPPLEMENT G?

The FDA product code for MYCOPLASMA SUPPLEMENT G is JSK.

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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.