Sun Biomedical Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sun Biomedical Laboratories, Inc. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Sun Biomedical Laboratories, Inc. has 17 FDA 510(k) cleared medical devices. Based in Cherry Hill, US.
Historical record: 17 cleared submissions from 1994 to 2003. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Sun Biomedical Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sun Biomedical Laboratories, Inc.
17 devices
Cleared
Aug 25, 2003
VISUALINE METHADONE DIPSTRIPTEST
Chemistry
279d
Cleared
May 06, 2003
VISUALINE CUP IV FOR DRUGS OF ABUSE TEST FOR QUALITATIVE DETERMINATION OF...
Toxicology
188d
Cleared
Apr 25, 2002
VISUALINE II (ALSO KNOWN AS SUNLINE) BARITURATES
Toxicology
135d
Cleared
Mar 20, 2002
VISUALINE BARBITURATES DIPSTRIP TEST
Toxicology
64d
Cleared
Jul 17, 2001
VISUALINE AMPHETAMINE DIPSTRIP ASSAY
Toxicology
63d
Cleared
May 17, 2001
VISUALINE II (ALSO KNOWN AS SUNLINE) AMPHETAMINE ASSAY
Toxicology
119d
Cleared
Dec 27, 1999
VISUALINE V DRUGS OF ABUSE DIPSTRIP PANEL FOR QUALITATIVE DETERMINATION OF...
Chemistry
74d
Cleared
Mar 01, 1999
VISUALINE II (ALSO KNOWN AS SUNLINE) PHENCYCLIDINE
Toxicology
125d
Cleared
Sep 04, 1998
VISUALINE II (ALSO KNOWN AS SUNLINE) METHADONE
Chemistry
147d
Cleared
Aug 12, 1997
VISUALINE II METHAMPHETIMINE
Toxicology
71d
Cleared
Oct 30, 1996
VISUALINE COMBO V (COCAINE/THC) TEST
Chemistry
51d
Cleared
Oct 18, 1996
VISUALINE D HCG
Chemistry
50d