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ELECSYS HCG AND BETA TEST SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K003178
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2000
Days to Decision
64 days
Submission Type
Summary

ELECSYS HCG AND BETA TEST SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K003178
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2000
Days to Decision
64 days
Submission Type
Summary