LIDOCAINE FLUORESCENT IMMUNOASSAY— 510(k) K822347

Name: FDA 510(k) clearance K822347
Creator: U.S. Food and Drug Administration
Published: 1982-08-25

Substantially Equivalent

American Diagnostic Corp.

FDA 510(k) clearance K822347 for LIDOCAINE FLUORESCENT IMMUNOASSAY, Substantially Equivalent on 1982-08-25. Applicant: American Diagnostic Corp.. Device class: 2.

Clearance details

Applicant: American Diagnostic Corp.
Product code: Code KLR
Device class: Class 2
Regulation: 21 CFR 862.3555
Advisory panel: Clinical Toxicology
Date received: 1982-08-06
Decision date: 1982-08-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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