DIAG. KIT FOR TOTAL ANTITHROMBIN III— 510(k) K771669

Name: FDA 510(k) clearance K771669
Creator: U.S. Food and Drug Administration
Published: 1977-11-09

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K771669 for DIAG. KIT FOR TOTAL ANTITHROMBIN III, Substantially Equivalent on 1977-11-09. Applicant: Abbott Laboratories. Device class: 2.

Clearance details

Applicant: Abbott Laboratories
Product code: Code JBQ
Device class: Class 2
Regulation: 21 CFR 864.7060
Advisory panel: Hematology
Date received: 1977-09-01
Decision date: 1977-11-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abbott Park, IL, US

Download summary PDF View on FDA.gov ↗

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