Company ยท US
Cybersonics, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2017. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 21, 2017 | K171024 | ShockPulse-SE Lithotripsy System Cybersonics, Inc. | FEO |
| Nov 13, 2014 | K142428 | Shock Pulse-SE Lithotripsy System CYBERWAND II Cybersonics, Inc. | FEO |
| Nov 26, 2013 | K132795 | CYBERWAND STERILE PROBE SET Cybersonics, Inc. | FFK |
| Jun 5, 2012 | K120303 | CYBERWAND DUAL ACTION ULTRASONIC LITHOTRIPSY SYSTEM Cybersonics, Inc. | FFK |
| Aug 30, 2010 | K102169 | CYBERWAND LITHOTRIPTER Cybersonics, Inc. | FFK |
| Oct 24, 2007 | K072422 | CYBERWAND STERILE PADS, MODEL: CW-RBPBX Cybersonics, Inc. | FFK |
| Dec 20, 2005 | K052135 | CYBERSONICS CYBERWAND DUAL PROBE LITHOTRIPTER Cybersonics, Inc. | FFK |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||