IMMULITE ACTH— 510(k) K960066

Substantially Equivalent

Diagnostic Products Corp.

FDA 510(k) clearance K960066 for IMMULITE ACTH, Substantially Equivalent on 1996-02-16. Applicant: Diagnostic Products Corp..

Clearance details

Applicant: Diagnostic Products Corp.
Product code: Code CKG
Advisory panel: Clinical Chemistry
Date received: 1996-01-05
Decision date: 1996-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

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