IMMULITE PROGESTERONE— 510(k) K935138

Substantially Equivalent

Diagnostic Products Corp.

FDA 510(k) clearance K935138 for IMMULITE PROGESTERONE, Substantially Equivalent on 1994-01-11. Applicant: Diagnostic Products Corp..

Clearance details

Applicant: Diagnostic Products Corp.
Product code: Code JLS
Advisory panel: Clinical Chemistry
Date received: 1993-10-28
Decision date: 1994-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

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