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PRECINORM UNIVERSAL PLUS AND PRECIPATH UNIVERSAL PLUS CONTROL SERA

Page Type
Cleared 510(K)
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)
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