LEECO TESTO-QUANT DIAG. KIT— 510(k) K813059

Substantially Equivalent

Leeco Diagnostics, Inc.

FDA 510(k) clearance K813059 for LEECO TESTO-QUANT DIAG. KIT, Substantially Equivalent on 1981-11-16. Applicant: Leeco Diagnostics, Inc..

Clearance details

Applicant: Leeco Diagnostics, Inc.
Product code: Code CDZ
Advisory panel: Clinical Chemistry
Date received: 1981-10-30
Decision date: 1981-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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