Sonicaid, Inc. - FDA 510(k) Cleared Devices
18
Total
17
Cleared
0
Denied
Sonicaid, Inc. has 17 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 17 cleared submissions from 1977 to 1988.
Browse the FDA 510(k) cleared devices submitted by Sonicaid, Inc. Filter by specialty or product code using the sidebar.
18 devices
Cleared
Feb 26, 1988
BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL
Cardiovascular
168d
Cleared
Aug 25, 1987
5 MHZ TRANSDUCER
Cardiovascular
88d
Cleared
May 06, 1987
VASOPULSE(TM)/MODEL 5000
Cardiovascular
219d
Cleared
Nov 17, 1986
VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBES
Cardiovascular
123d
Cleared
Jul 14, 1986
VASOVIEW DUPLEX IMAGING SYSTEM
Radiology
103d
Cleared
May 16, 1985
VASOSCREEN IMPEDANCE PLETHYSMOGRAPH
Cardiovascular
58d
Cleared
Jan 27, 1984
VASOSCAN
Cardiovascular
74d
Cleared
Dec 01, 1983
PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH
Cardiovascular
136d
Cleared
Nov 28, 1983
SONICOMP
Obstetrics & Gynecology
52d
Cleared
Oct 27, 1983
SONICAID MODEL D206E AIR EMBOLI-DETECT
Toxicology
72d
Cleared
Jun 30, 1983
MODEL FM5
Obstetrics & Gynecology
64d
Cleared
Oct 20, 1981
MODEL AP 180 MINI-MONITOR
Obstetrics & Gynecology
69d
Cleared
Jan 28, 1981
ULTRASONIC STETHOSCOPE
Radiology
36d
Cleared
May 14, 1980
FETAL HEART DETECTOR #'S D102 & D102R
Obstetrics & Gynecology
29d
Cleared
May 14, 1980
FETAL HEART DETECTOR #D206
Obstetrics & Gynecology
29d
Cleared
May 11, 1979
INTRAUTERINE CATHETER TIP
Radiology
32d
Cleared
May 09, 1978
FETAL MONITORING SYSTEM
Obstetrics & Gynecology
43d
Cleared
Aug 03, 1977
FETAL MONITORING SYS. MODEL FM3R
Obstetrics & Gynecology
8d