Last synced on 18 July 2025 at 11:06 pm

TIA CRP TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914155
510(k) Type
Traditional
Applicant
CRESTAT DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/1992
Days to Decision
121 days
Submission Type
Statement

TIA CRP TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914155
510(k) Type
Traditional
Applicant
CRESTAT DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/1992
Days to Decision
121 days
Submission Type
Statement