IN VITRO NEONATAL T4— 510(k) K780854

Substantially Equivalent

Clinical Assays, Inc.

FDA 510(k) clearance K780854 for IN VITRO NEONATAL T4, Substantially Equivalent on 1978-07-27. Applicant: Clinical Assays, Inc.. Device class: 2.

Clearance details

Applicant: Clinical Assays, Inc.
Product code: Code CDX
Device class: Class 2
Regulation: 21 CFR 862.1700
Advisory panel: Clinical Chemistry
Date received: 1978-05-22
Decision date: 1978-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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