ANTISERUM TO HUMAN CERULOPLASMIN— 510(k) K790714

Substantially Equivalent

Kent Laboratories, Inc.

FDA 510(k) clearance K790714 for ANTISERUM TO HUMAN CERULOPLASMIN, Substantially Equivalent on 1979-08-16. Applicant: Kent Laboratories, Inc..

Clearance details

Applicant: Kent Laboratories, Inc.
Product code: Code DDB
Advisory panel: Immunology
Date received: 1979-04-12
Decision date: 1979-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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