Cybersonics, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Cybersonics, Inc. has 7 FDA 510(k) cleared medical devices. Based in Erie, US.
Historical record: 7 cleared submissions from 2005 to 2017. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Cybersonics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cybersonics, Inc.
7 devices
Cleared
Aug 21, 2017
ShockPulse-SE Lithotripsy System
Gastroenterology & Urology
138d
Cleared
Nov 13, 2014
Shock Pulse-SE Lithotripsy System CYBERWAND II
Gastroenterology & Urology
76d
Cleared
Nov 26, 2013
CYBERWAND STERILE PROBE SET
Gastroenterology & Urology
81d
Cleared
Jun 05, 2012
CYBERWAND DUAL ACTION ULTRASONIC LITHOTRIPSY SYSTEM
Gastroenterology & Urology
125d
Cleared
Aug 30, 2010
CYBERWAND LITHOTRIPTER
Gastroenterology & Urology
28d
Cleared
Oct 24, 2007
CYBERWAND STERILE PADS, MODEL: CW-RBPBX
Gastroenterology & Urology
57d
Cleared
Dec 20, 2005
CYBERSONICS CYBERWAND DUAL PROBE LITHOTRIPTER
Gastroenterology & Urology
137d