TY RIA KIT, AUTOMATED ASSAY SYSTEM— 510(k) K790477

Name: FDA 510(k) clearance K790477
Creator: U.S. Food and Drug Administration
Published: 1979-04-26

Substantially Equivalent

E. R. Squibb & Sons, Inc.

FDA 510(k) clearance K790477 for TY RIA KIT, AUTOMATED ASSAY SYSTEM, Substantially Equivalent on 1979-04-26. Applicant: E. R. Squibb & Sons, Inc.. Device class: 2.

Clearance details

Applicant: E. R. Squibb & Sons, Inc.
Product code: Code CDX
Device class: Class 2
Regulation: 21 CFR 862.1700
Advisory panel: Clinical Chemistry
Date received: 1979-03-09
Decision date: 1979-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

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