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U.S. DIAGNOSTICS LIQUID CK ISOENZYME CONTROL

Page Type
Cleared 510(K)
510(k) Number
K870738
510(k) Type
Traditional
Applicant
U. S. DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/1987
Days to Decision
47 days

U.S. DIAGNOSTICS LIQUID CK ISOENZYME CONTROL

Page Type
Cleared 510(K)
510(k) Number
K870738
510(k) Type
Traditional
Applicant
U. S. DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/1987
Days to Decision
47 days