IN VITRO THEOPHYLLINE RIA TEST— 510(k) K772017

Substantially Equivalent

Clinical Assays, Inc.

FDA 510(k) clearance K772017 for IN VITRO THEOPHYLLINE RIA TEST, Substantially Equivalent on 1978-03-27. Applicant: Clinical Assays, Inc..

Clearance details

Applicant: Clinical Assays, Inc.
Product code: Code KLS
Advisory panel: Clinical Toxicology
Date received: 1977-10-26
Decision date: 1978-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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