Zonare Medical Systems, Inc. is one of 18478 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zonare Medical Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ZONARE ZS3 Diagnostic Ultrasound System, ZONARE ZS3 and Z.Onepro Diagnostic Ultrasound System, ZONARE ZS3 DIAGNOSTIC ULTRASOUND SYSTEM
6
Total
6
Cleared
0
Denied
Zonare Medical Systems, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 6 cleared submissions from 2008 to 2015. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Zonare Medical Systems, 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 - Zonare Medical Systems, Inc.
6 devices
Cleared
May 15, 2015
ZONARE ZS3 Diagnostic Ultrasound System
Radiology
14d
Cleared
Mar 04, 2015
ZONARE ZS3 and Z.Onepro Diagnostic Ultrasound System
Radiology
29d
Cleared
Jul 18, 2014
ZONARE ZS3 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
29d
Cleared
Apr 13, 2012
ZONARE ZS3 DIAGNOSTIC UNLTRASOUND SYSTEM
Radiology
36d
Cleared
Jun 25, 2010
Z.ONE ULTRA ULTRASOUND SYSTEM
Radiology
67d
Cleared
Oct 08, 2008
ZONARE ULTRA ULTRASOUND SYSTEM
Radiology
55d