IN VITRO GENTAMICIN RADIOIMMUNOASSY TEST— 510(k) K780709

Substantially Equivalent

Clinical Assays, Inc.

FDA 510(k) clearance K780709 for IN VITRO GENTAMICIN RADIOIMMUNOASSY TEST, Substantially Equivalent on 1978-05-12. Applicant: Clinical Assays, Inc..

Clearance details

Applicant: Clinical Assays, Inc.
Advisory panel: Unknown
Date received: 1978-04-26
Decision date: 1978-05-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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