IN VITRO THEOPHYLLINE RIA TEST— 510(k) K772017

Name: FDA 510(k) clearance K772017
Creator: U.S. Food and Drug Administration
Published: 1978-03-27

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.. Device class: 2.

Clearance details

Applicant: Clinical Assays, Inc.
Product code: Code KLS
Device class: Class 2
Regulation: 21 CFR 862.3880
Advisory panel: Clinical Toxicology
Date received: 1977-10-26
Decision date: 1978-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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