Cybersonics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K171024ShockPulse-SE Lithotripsy SystemAugust 21, 2017
K142428Shock Pulse-SE Lithotripsy System CYBERWAND IINovember 13, 2014
K132795CYBERWAND STERILE PROBE SETNovember 26, 2013
K120303CYBERWAND DUAL ACTION ULTRASONIC LITHOTRIPSY SYSTEMJune 5, 2012
K102169CYBERWAND LITHOTRIPTERAugust 30, 2010
K072422CYBERWAND STERILE PADS, MODEL: CW-RBPBXOctober 24, 2007
K052135CYBERSONICS CYBERWAND DUAL PROBE LITHOTRIPTERDecember 20, 2005