ABBOTT VERTEX ANALYZER— 510(k) K920559

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K920559 for ABBOTT VERTEX ANALYZER, Substantially Equivalent on 1992-03-19. Applicant: Abbott Laboratories.

Clearance details

Applicant: Abbott Laboratories
Product code: Code JJJ
Advisory panel: Clinical Chemistry
Date received: 1992-02-07
Decision date: 1992-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abbott Park, IL, US

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