LEECO LH-QUANT DIAGNOSTIC KIT— 510(k) K810662

Substantially Equivalent

Leeco Diagnostics, Inc.

FDA 510(k) clearance K810662 for LEECO LH-QUANT DIAGNOSTIC KIT, Substantially Equivalent on 1981-03-31. Applicant: Leeco Diagnostics, Inc..

Clearance details

Applicant: Leeco Diagnostics, Inc.
Product code: Code CEP
Advisory panel: Clinical Chemistry
Date received: 1981-03-11
Decision date: 1981-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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