ABBOTT LABORATORIES PROLACTIN EIA— 510(k) K822759

Name: FDA 510(k) clearance K822759
Creator: U.S. Food and Drug Administration
Published: 1982-10-21

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K822759 for ABBOTT LABORATORIES PROLACTIN EIA, Substantially Equivalent on 1982-10-21. Applicant: Abbott Laboratories. Device class: 1.

Clearance details

Applicant: Abbott Laboratories
Product code: Code CFT
Device class: Class 1
Regulation: 21 CFR 862.1625
Advisory panel: Clinical Chemistry
Date received: 1982-09-14
Decision date: 1982-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abbott Park, IL, US

Download summary PDF View on FDA.gov ↗

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