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CREATINE KINASE REAGENT

Page Type
Cleared 510(K)
510(k) Number
K803301
510(k) Type
Traditional
Applicant
GILFORD DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/1981
Days to Decision
17 days

CREATINE KINASE REAGENT

Page Type
Cleared 510(K)
510(k) Number
K803301
510(k) Type
Traditional
Applicant
GILFORD DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/1981
Days to Decision
17 days