Pan Probe Biotech, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pan Probe Biotech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LIVESURE HCG URINARY PREGNANCY TEST STRIP AND TEST CARD, LIVESURE METHADONE SCREEN TESTS, LIVESURE PHENECYCLINE (PCP) SCREEN TESTS
10
Total
10
Cleared
0
Denied
Pan Probe Biotech, Inc. has 10 FDA 510(k) cleared toxicology devices. Based in San Diego, US.
Historical record: 10 cleared submissions from 2001 to 2002.
Browse the complete list of FDA 510(k) cleared toxicology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by California Department of Health Services as regulatory consultant.
FDA 510(k) Regulatory Record - Pan Probe Biotech, Inc.
10 devices
Cleared
Jul 15, 2002
LIVESURE HCG URINARY PREGNANCY TEST STRIP AND TEST CARD
Chemistry
111d
Cleared
Nov 26, 2001
LIVESURE METHADONE SCREEN TESTS
Toxicology
11d
Cleared
Jul 20, 2001
LIVESURE PHENECYCLINE (PCP) SCREEN TESTS
Toxicology
15d
Cleared
Jul 20, 2001
LIVESURE BENZODIAZEPINES SCREEN TESTS
Toxicology
11d
Cleared
Jul 20, 2001
LIVESURE BARBITURATES SCREEN TEST
Toxicology
11d
Cleared
Jun 08, 2001
LIVESURE AMPHETAMINE SCREEN TEST
Toxicology
14d
Cleared
Jun 08, 2001
LIVESURE METHAMPHETAMINE SCREEN TESTS
Toxicology
14d
Cleared
Apr 17, 2001
LIVESURE COCAINE SCREEN TEST
Toxicology
15d
Cleared
Apr 13, 2001
LIVESURE MORPHINE SCREEN TEST
Toxicology
9d
Cleared
Feb 05, 2001
LIVESURE THC SCREEN TEST
Toxicology
34d