DIRECT LDL— 510(k) K981303

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K981303 for DIRECT LDL, Substantially Equivalent on 1998-08-03. Applicant: Abbott Laboratories.

Clearance details

Applicant: Abbott Laboratories
Product code: Code MRR
Advisory panel: Clinical Chemistry
Date received: 1998-04-10
Decision date: 1998-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irving, TX, US

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