Biophor Diagnostics, Inc. is one of 4964 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biophor Diagnostics, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Biophor Diagnostics, Inc. has 7 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Historical record: 7 cleared submissions from 2013 to 2015. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Biophor Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biophor Diagnostics, Inc.
7 devices
Cleared
Sep 18, 2015
Rapidfret Oral Fluid Assay for Methamphetamine, Rapidfret Oral Fluid...
Toxicology
396d
Cleared
Jul 24, 2015
RAPIDFRET ORAL FLUID ASSAY FOR COCAINE, RAPIDFRET ORAL FLUID COCAINE...
Toxicology
354d
Cleared
May 20, 2015
RAPIDFRET ORAL FLUID ASSAY FOR AMPHETAMINE, RAPIDFRET ORAL FLUID AMPHETAMINE...
Toxicology
324d
Cleared
Dec 18, 2014
RAPIDFRET ORAL FLUID ASSAY FOR MDMA, RAPIDFRET ORAL FLUID CALIBRATORS,...
Chemistry
447d
Cleared
Jan 24, 2014
RAPIDFRET ORAL FLUID ASSAY FOR OPIATES
Toxicology
58d
Cleared
Oct 18, 2013
RAPIDFRET ORAL FLUID ASSAY FOR THC, THC CALIBRATOR SET, THC CONTROL SET,...
Toxicology
102d
Cleared
Apr 25, 2013
RAPIDFRET ORAL FLUID ASSAY FOR PCP, PCP CALIBRATOR SET, PCP CONTROL SET AND...
Toxicology
233d