Starplex Scientific, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Starplex Scientific, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Starplex Scientific, Inc. has 11 FDA 510(k) cleared medical devices. Based in Etobicoke, Ontario, CA.
Historical record: 11 cleared submissions from 1992 to 2003. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Starplex Scientific, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Starplex Scientific, Inc.
11 devices
Cleared
Aug 13, 2003
MODIFICATION TO MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEM
Microbiology
22d
Cleared
Feb 27, 2003
STARTOX DRUG OF ABUSE SCREENING TEST (4)
Toxicology
219d
Cleared
Jun 10, 2002
STARTOX DRUG OF ABUSE SCREENING TEST
Toxicology
74d
Cleared
Sep 18, 1996
MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEM
Microbiology
58d
Cleared
Apr 03, 1996
STARSWAB CULTURE COLLECTION AND TRANSPORT SYSTEM
Microbiology
22d
Cleared
Feb 16, 1995
KULTSURE/STARSWAB ANAEROBIC TRANSPORT SYSTEM
Microbiology
139d
Cleared
Mar 01, 1993
VACUPLUS TUBES WITH GREEN STOPPERS
Chemistry
185d
Cleared
Mar 01, 1993
VACUPLUS TUBES WITH LAVANDER STOPPERS
Chemistry
185d
Cleared
Mar 01, 1993
VACUPLUS TUBES WITH GREY STOPPERS
Chemistry
185d
Cleared
Feb 08, 1993
VACUPLUS(R) STAR-SEP(TM)
Chemistry
164d
Cleared
Dec 28, 1992
VACUPLUS TUBES WITH BRICK RED STOPPERS
Chemistry
122d