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CREATININE ASSAY KIT-KINETIC OR ENDPOINT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842159
510(k) Type
Traditional
Applicant
DIAGNOSTIC CHEMICALS, LTD. (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1984
Days to Decision
78 days

CREATININE ASSAY KIT-KINETIC OR ENDPOINT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842159
510(k) Type
Traditional
Applicant
DIAGNOSTIC CHEMICALS, LTD. (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1984
Days to Decision
78 days