Sonomed, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Sonomed, Inc. has 8 FDA 510(k) cleared medical devices. Based in Lake Success, US.
Historical record: 8 cleared submissions from 1992 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Sonomed, Inc. Filter by specialty or product code using the sidebar.
8 devices
Cleared
May 02, 2017
AXIS Image Management System
Ophthalmic
19d
Cleared
Apr 01, 2014
VUPAD
Radiology
64d
Cleared
Apr 09, 2010
MASTER-VU A-SCAN, MV4500
Radiology
71d
Cleared
Sep 24, 2009
PACSCAN PLUS, MODELS 300P AND 300AP
Radiology
28d
Cleared
Dec 19, 2007
MASTER-VU
Radiology
36d
Cleared
Apr 11, 2006
VUMAX
Radiology
33d
Cleared
Apr 13, 2004
E-Z SCAN AB5500+
Radiology
29d
Cleared
Dec 08, 1992
SONOMED 4000P ULTRASONIC PACHYMETER
Radiology
104d