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RAPIDFRET ORAL FLUID ASSAY FOR THC, THC CALIBRATOR SET, THC CONTROL SET, COLLECTOR

Page Type
Cleared 510(K)
510(k) Number
K132096
510(k) Type
Traditional
Applicant
BIOPHOR DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2013
Days to Decision
102 days
Submission Type
Summary

RAPIDFRET ORAL FLUID ASSAY FOR THC, THC CALIBRATOR SET, THC CONTROL SET, COLLECTOR

Page Type
Cleared 510(K)
510(k) Number
K132096
510(k) Type
Traditional
Applicant
BIOPHOR DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2013
Days to Decision
102 days
Submission Type
Summary