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IN VITRO DIAG. FOR URIC ACID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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