HUMAN CERULOPLASMIN— 510(k) K791339

Substantially Equivalent

Beckman Instruments, Inc.

FDA 510(k) clearance K791339 for HUMAN CERULOPLASMIN, Substantially Equivalent on 1979-08-16. Applicant: Beckman Instruments, Inc..

Clearance details

Applicant: Beckman Instruments, Inc.
Product code: Code DDB
Advisory panel: Immunology
Date received: 1979-07-16
Decision date: 1979-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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