RHEUMADX LATEX AGGLUTINATION RHEUMATOID— 510(k) K843896

Substantially Equivalent

Diagnostic Products Corp.

FDA 510(k) clearance K843896 for RHEUMADX LATEX AGGLUTINATION RHEUMATOID, Substantially Equivalent on 1984-10-25. Applicant: Diagnostic Products Corp..

Clearance details

Applicant: Diagnostic Products Corp.
Product code: Code DHR
Advisory panel: Immunology
Date received: 1984-10-03
Decision date: 1984-10-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

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