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PRECINORM UNIVERSAL PLUS AND PRECIPATH UNIVERSAL PLUS CONTROL SERA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993360
510(k) Type
Traditional
Applicant
Roche Diagnostics Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1999
Days to Decision
49 days
Submission Type
Summary

PRECINORM UNIVERSAL PLUS AND PRECIPATH UNIVERSAL PLUS CONTROL SERA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993360
510(k) Type
Traditional
Applicant
Roche Diagnostics Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1999
Days to Decision
49 days
Submission Type
Summary