Last synced on 23 September 2022 at 11:05 pm

OMNI C ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013373
510(k) Type
Special
Applicant
ROCHE DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2001
Days to Decision
22 days
Submission Type
Summary

OMNI C ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013373
510(k) Type
Special
Applicant
ROCHE DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2001
Days to Decision
22 days
Submission Type
Summary