Last synced on 6 June 2025 at 11:06 pm

RAPIDFRET ORAL FLUID ASSAY FOR AMPHETAMINE, RAPIDFRET ORAL FLUID AMPHETAMINE CALIBRATOR SET, RAPIDFRET ORAL FLUID AMPHETAMINE CONTROL SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141748
510(k) Type
Traditional
Applicant
BIOPHOR DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/2015
Days to Decision
324 days
Submission Type
Summary

RAPIDFRET ORAL FLUID ASSAY FOR AMPHETAMINE, RAPIDFRET ORAL FLUID AMPHETAMINE CALIBRATOR SET, RAPIDFRET ORAL FLUID AMPHETAMINE CONTROL SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141748
510(k) Type
Traditional
Applicant
BIOPHOR DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/2015
Days to Decision
324 days
Submission Type
Summary