Deseret Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Deseret Medical, Inc. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Deseret Medical, Inc. has 20 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 20 cleared submissions from 1979 to 1991. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Deseret Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Deseret Medical, Inc.
20 devices
Cleared
Nov 27, 1991
VESSEL DILATOR
Cardiovascular
141d
Cleared
Dec 14, 1990
SAFE SYTE I.V. CATHETER PLACEMENT UNIT
General Hospital
64d
Cleared
Nov 08, 1990
VIALON OBTURATOR
General Hospital
63d
Cleared
Oct 04, 1990
INSYTE-A ARTERIAL CATHETERIZATION UNIT
General Hospital
28d
Cleared
Jun 18, 1990
DESERET OPTIMA INTRAVASCULAR CATHETER
General Hospital
160d
Cleared
May 18, 1990
DESERET MULTILUMEN SUBCLAVIAN CATHETER
General Hospital
233d
Cleared
Apr 09, 1990
DESERET INTRAVASCULAR CATHETER
General Hospital
195d
Cleared
Oct 17, 1989
DISPOSABLE CATHETER PRESSURE TRANSDUCER
Cardiovascular
133d
Cleared
Jun 22, 1989
DESERET PRN ADAPTER
General & Plastic Surgery
51d
Cleared
Jul 18, 1988
LUER-LOK MULTIFLO ADAPTER
General Hospital
12d
Cleared
Jul 18, 1988
MULTIFLO ADAPTER
General Hospital
12d
Cleared
Jun 23, 1988
DESERET SUBCLAVIAN HEMODIALYSIS CATHETER
Gastroenterology & Urology
65d