ABBOTT A-GENT IRON REAGENT KIT— 510(k) K873120

Name: FDA 510(k) clearance K873120
Creator: U.S. Food and Drug Administration
Published: 1987-08-25

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K873120 for ABBOTT A-GENT IRON REAGENT KIT, Substantially Equivalent on 1987-08-25. Applicant: Abbott Laboratories. Device class: 1.

Clearance details

Applicant: Abbott Laboratories
Product code: Code CFM
Device class: Class 1
Regulation: 21 CFR 862.1410
Advisory panel: Clinical Chemistry
Date received: 1987-08-10
Decision date: 1987-08-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irving, TX, US

Download summary PDF View on FDA.gov ↗

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