LEECO GLYCO-HEMOGLOBIN DIAG. TEST KIT— 510(k) K801289

Substantially Equivalent

Leeco Diagnostics, Inc.

FDA 510(k) clearance K801289 for LEECO GLYCO-HEMOGLOBIN DIAG. TEST KIT, Substantially Equivalent on 1980-06-30. Applicant: Leeco Diagnostics, Inc..

Clearance details

Applicant: Leeco Diagnostics, Inc.
Product code: Code LCP
Advisory panel: Hematology
Date received: 1980-05-30
Decision date: 1980-06-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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