Sonomed, Inc. is one of 18471 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sonomed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AXIS Image Management System, VUPAD, MASTER-VU A-SCAN, MV4500
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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Sonomed, Inc.
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