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ROCHE UNIMATE HDL DIRECT REAGENT, ROCHE CALIBRATOR HDL DIRECT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971902
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/1997
Days to Decision
24 days
Submission Type
Statement

ROCHE UNIMATE HDL DIRECT REAGENT, ROCHE CALIBRATOR HDL DIRECT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971902
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/1997
Days to Decision
24 days
Submission Type
Statement