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CREATINE KINASE TEST (CK) ITEM NUMBER 65411

Page Type
Cleared 510(K)
510(k) Number
K903333
510(k) Type
Traditional
Applicant
EM DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1990
Days to Decision
23 days

CREATINE KINASE TEST (CK) ITEM NUMBER 65411

Page Type
Cleared 510(K)
510(k) Number
K903333
510(k) Type
Traditional
Applicant
EM DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1990
Days to Decision
23 days