Ulster Scientific, Inc. is one of 5123 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ulster Scientific, Inc. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Ulster Scientific, Inc. has 20 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 20 cleared submissions from 1980 to 1994.
Browse the FDA 510(k) cleared devices submitted by Ulster Scientific, Inc. Filter by specialty or product code using the sidebar.
Ulster Scientific, Inc. — FDA 510(k) Products and Clearance History
20 devices
Cleared
Jun 22, 1994
FEATHER-TOUCH SINGLE-STICK DEVICE
General & Plastic Surgery
20d
Cleared
Mar 27, 1992
UNISTIK
General & Plastic Surgery
50d
Cleared
Jul 19, 1990
EPC ELECTRONIC PIPETTING SYSTEM
Chemistry
37d
Cleared
Feb 16, 1990
AUTOPEN
General Hospital
134d
Cleared
Aug 18, 1989
THE AUTOLET LITE
General & Plastic Surgery
31d
Cleared
Feb 14, 1989
AIR DISPLACEMENT PIPETTE
Chemistry
48d
Cleared
Feb 17, 1988
UNISTEP CAPILLARY BLOOD COLLECTION SYSTEM
Hematology
48d
Cleared
Jun 18, 1987
NEUROTIPS(TM)
Neurology
57d
Cleared
Mar 23, 1987
WINPETTE
Hematology
5d
Cleared
Mar 17, 1987
ACCUPEN(R)
General Hospital
68d
Cleared
Dec 16, 1986
USI AUTOJECT INSULIN SYRINGE
General Hospital
11d
Cleared
Apr 29, 1986
NEONATAL UNILET
General & Plastic Surgery
27d
Cleared
Apr 14, 1986
DISPETTE II
Hematology
35d
Cleared
Apr 07, 1986
DIAMATIC, AUTOMATIC INSULIN INJECTOR
General Hospital
69d
Cleared
Dec 23, 1985
MICRO-MAT SYSTEM
Hematology
12d
Cleared
Jun 06, 1985
PRECI-JET 50
General Hospital
73d
Cleared
Sep 20, 1984
UNILET LANCET
General Hospital
72d
Cleared
Oct 31, 1983
GLUCOKEY
Hematology
202d
Cleared
May 09, 1983
WESTERGREN DISPETTE FOR ESR
Hematology
27d
Cleared
Oct 10, 1980
AUTOLET
Hematology
72d