Last synced on 27 June 2025 at 11:06 pm

TINA-QUANT CERULOPLASMIN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091741
510(k) Type
Traditional
Applicant
Roche Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/2010
Days to Decision
275 days
Submission Type
Summary

TINA-QUANT CERULOPLASMIN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091741
510(k) Type
Traditional
Applicant
Roche Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/2010
Days to Decision
275 days
Submission Type
Summary