LDH (L-P) REAGENT— 510(k) K800120

Substantially Equivalent

Gilford Diagnostics

FDA 510(k) clearance K800120 for LDH (L-P) REAGENT, Substantially Equivalent on 1980-02-13. Applicant: Gilford Diagnostics.

Clearance details

Applicant: Gilford Diagnostics
Product code: Code CFJ
Advisory panel: Clinical Chemistry
Date received: 1980-01-18
Decision date: 1980-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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