Syntron Bioresearch, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Syntron Bioresearch, Inc. - FDA 510(k) Cleared Devices
26
Total
26
Cleared
0
Denied
Syntron Bioresearch, Inc. has 26 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 26 cleared submissions from 1987 to 1999. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Syntron Bioresearch, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Syntron Bioresearch, Inc.
26 devices
Cleared
Oct 29, 1999
QUICKSTRIP ONE STEP OPIATES TEST
Toxicology
14d
Cleared
Oct 29, 1999
QUICKPAC II ONE STEP OPIATES TEST
Toxicology
14d
Cleared
Sep 20, 1999
QUICKPAC II ONE STEP COCAINE TEST
Toxicology
13d
Cleared
Sep 02, 1999
DRUGCHECK X MULTIDRUG SCREENING DEVICE
Toxicology
17d
Cleared
Jul 22, 1999
QUIKSTRIP ONE STEP COCAINE ASSAY (COCAINE AND COCAINE METABOLITE TEST SYSTEM
Toxicology
22d
Cleared
Jun 24, 1999
QUIKSTRIP DIPSCAN X MULTIDRUG SCREENING DEVICE
Toxicology
142d
Cleared
Nov 18, 1998
BESURE PLUS ONE-STEP HOME OVULATION PREDICTOR KIT
Chemistry
75d
Cleared
May 26, 1998
QUIKPAC II ONE STEP PHENCYCLIDINE (PCP) TEST
Toxicology
47d
Cleared
May 07, 1998
QUIKSTRIP ONE STEP PHENCYCLIDINE (PCP) TEST
Toxicology
50d
Cleared
Mar 03, 1998
QUICKPAC II ONE STEP BARBITURATE TEST
Toxicology
34d
Cleared
Feb 12, 1998
QUIKSTRIP ONE STEP BARBITURATE TEST
Toxicology
57d
Cleared
Feb 28, 1997
QUIKSTRIP ONESTEP MARIJUANA (THC) TEST
Toxicology
169d