Sonocine, Inc. is one of 24586 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sonocine, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SONOCINE ADJUNCTIVE BREAST ULTRASOUND SYSTEM (ABU), MODEL 100
1
Total
1
Cleared
0
Denied
Sonocine, Inc. has 1 FDA 510(k) cleared medical devices. Based in Reno, US.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Sonocine, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Sonocine, Inc.
1 devices