IMMULITE RUBELLA IGG— 510(k) K963613

Substantially Equivalent

Diagnostic Products Corp.

FDA 510(k) clearance K963613 for IMMULITE RUBELLA IGG, Substantially Equivalent on 1997-04-02. Applicant: Diagnostic Products Corp..

Clearance details

Applicant: Diagnostic Products Corp.
Product code: Code LFX
Advisory panel: Microbiology
Date received: 1996-09-10
Decision date: 1997-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

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