ABBOTT RF EIA DIAGNOSTIC KIT— 510(k) K850373

Name: FDA 510(k) clearance K850373
Creator: U.S. Food and Drug Administration
Published: 1985-03-01

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K850373 for ABBOTT RF EIA DIAGNOSTIC KIT, Substantially Equivalent on 1985-03-01. Applicant: Abbott Laboratories. Device class: 2.

Clearance details

Applicant: Abbott Laboratories
Product code: Code DHR
Device class: Class 2
Regulation: 21 CFR 866.5775
Advisory panel: Immunology
Date received: 1985-01-31
Decision date: 1985-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abbott Park, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.