Medasonics, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Medasonics, Inc. has 19 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1978 to 1999. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medasonics, Inc. Filter by specialty or product code using the sidebar.
19 devices
Cleared
Dec 28, 1999
CADENCE DOPPLER ULTRASOUND SYSTEM
Radiology
246d
Cleared
Jan 21, 1997
NEUROGUARD TRANSCRANIAL DOPPLER ULTRASOUND SYSTEM
Radiology
187d
Cleared
Aug 08, 1996
FIRST BEAT/CARDIO BEAT/CALC
Radiology
141d
Cleared
Dec 03, 1992
CEREBROVASCULAR DIAGNOSTIC SYSTEM
Radiology
401d
Cleared
Jun 20, 1991
OBTRASOUND STETHOSCOPE FETAL CALC
Radiology
78d
Cleared
Sep 21, 1988
MEDACORD PVL, PERSONAL VASCULAR LABORATORY
Radiology
131d
Cleared
Aug 14, 1987
TRANSPECT TRANSCRANIAL DOPPLER
Radiology
59d
Cleared
Feb 10, 1986
MODEL 5320 TED SEQUENTIAL COMP. DE. COMP. LIMB SLE
Cardiovascular
77d
Cleared
Nov 14, 1983
VASCULAR LABORATORY TREADMILL VT1
Physical Medicine
33d
Cleared
Jun 24, 1983
BF24 DOPPLER MODEL P872 AND P874
Radiology
46d
Cleared
Jun 16, 1983
VASCULAB BLOOD PRESSURE CUFF
Cardiovascular
48d
Cleared
Apr 21, 1982
VASCULAB SPECTRUM ANALYZER #SP25
Cardiovascular
22d