MYCOPLASMA SUPPLEMENT P— 510(k) K800254

Substantially Equivalent

Oxoid U.S.A., Inc.

FDA 510(k) clearance K800254 for MYCOPLASMA SUPPLEMENT P, Substantially Equivalent on 1980-03-12. Applicant: Oxoid U.S.A., Inc.. Device class: 1.

Clearance details

Applicant: Oxoid U.S.A., Inc.
Product code: Code JSK
Device class: Class 1
Regulation: 21 CFR 866.2450
Advisory panel: Microbiology
Date received: 1980-02-06
Decision date: 1980-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.