Last synced on 25 January 2026 at 3:41 am

TINA-QUANT MYOGLOBIN GEN.2 TEST SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061683
510(k) Type
Traditional
Applicant
Roche Diagnostics Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2006
Days to Decision
36 days
Submission Type
Summary

TINA-QUANT MYOGLOBIN GEN.2 TEST SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061683
510(k) Type
Traditional
Applicant
Roche Diagnostics Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2006
Days to Decision
36 days
Submission Type
Summary