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N-ASSAY TIA APO A1 TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964292
510(k) Type
Traditional
Applicant
CRESTAT DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1997
Days to Decision
276 days
Submission Type
Statement

N-ASSAY TIA APO A1 TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964292
510(k) Type
Traditional
Applicant
CRESTAT DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1997
Days to Decision
276 days
Submission Type
Statement