Medsonics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medsonics - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Medsonics has 4 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 4 cleared submissions from 1976 to 1977. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medsonics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medsonics
4 devices
Cleared
May 26, 1977
PROBE, BLOOD FLOW DETECTOR PLUG-IN
Obstetrics & Gynecology
10d
Cleared
Feb 24, 1977
AMPLIFIER, PHOTOPULSE, MODEL PA13
Cardiovascular
7d
Cleared
Oct 13, 1976
CONTINUOUS WAVE DOPPLER
Cardiovascular
12d
Cleared
Oct 06, 1976
CONTINUOUS WAVE DOPPLER ULTRASOUND
Obstetrics & Gynecology
9d