GENTAMICIN FLUORESCENT IMMUNOASSAY— 510(k) K813539

Name: FDA 510(k) clearance K813539
Creator: U.S. Food and Drug Administration
Published: 1981-12-31

Substantially Equivalent

American Diagnostic Corp.

FDA 510(k) clearance K813539 for GENTAMICIN FLUORESCENT IMMUNOASSAY, Substantially Equivalent on 1981-12-31. Applicant: American Diagnostic Corp.. Device class: 2.

Clearance details

Applicant: American Diagnostic Corp.
Product code: Code LCQ
Device class: Class 2
Regulation: 21 CFR 862.3450
Advisory panel: Clinical Toxicology
Date received: 1981-12-21
Decision date: 1981-12-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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