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IN VITRO DIAG. FOR URIC ACID

Page Type
Cleared 510(K)
510(k) Number
K770767
510(k) Type
Traditional
Applicant
SMITH KLINE DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/1977
Days to Decision
68 days

IN VITRO DIAG. FOR URIC ACID

Page Type
Cleared 510(K)
510(k) Number
K770767
510(k) Type
Traditional
Applicant
SMITH KLINE DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/1977
Days to Decision
68 days