Drial Consultants, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Drial Consultants, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Drial Consultants, Inc. has 13 FDA 510(k) cleared toxicology devices. Based in Menlo Park, US.
Historical record: 13 cleared submissions from 1997 to 1998.
Browse the complete list of FDA 510(k) cleared toxicology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Drial Consultants, Inc.
13 devices
Cleared
Feb 25, 1998
QUIKSTRIP ONE STEP BENZODIAZEPINE TEST
Toxicology
180d
Cleared
Feb 24, 1998
QUIKPAC II ONE STEP BENZODIAZEPINE TEST
Toxicology
173d
Cleared
Oct 02, 1997
ONE STEP URINE DRUG OF ABUSE BARBITURATE TEST
Toxicology
48d
Cleared
Aug 28, 1997
QUIKPAC II ONE STEP COCAINE TEST
Toxicology
87d
Cleared
Aug 20, 1997
QUIKSTRIP ONE STEP OPIATES TEST
Toxicology
41d
Cleared
Aug 08, 1997
QUIKPAC II ONE STEP OPIATE TEST
Toxicology
43d
Cleared
Jul 14, 1997
QUIKSTRIP ONE STEP COCAINE TEST
Toxicology
48d
Cleared
Jun 26, 1997
QUIKSTRIP ONE STEP METHAMPHETAMINE
Toxicology
143d
Cleared
May 30, 1997
QUIKSTRIP ONE STEP AMPHETAMINE TEST
Toxicology
58d
Cleared
May 14, 1997
QUIKPAC II ONE STEP AMPHETAMINE TEST
Toxicology
49d
Cleared
May 13, 1997
QUICKPAC II ONE STEP METHAMPHETAMINE TEST
Toxicology
75d
Cleared
Apr 08, 1997
ONE STEP URINE DRUG OF ABUSE METHAMPHETAMINE TEST
Toxicology
75d
Cleared
Feb 20, 1997
QUICKPAC II ONE STEP MARIJUANA (THC) TEST
Toxicology
189d