FDA 510(k) Applications Submitted by LORI COLVIN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K120303 | 02/01/2012 | CYBERWAND DUAL ACTION ULTRASONIC LITHOTRIPSY SYSTEM | CYBERSONICS, INC. |
| K132795 | 09/06/2013 | CYBERWAND STERILE PROBE SET | CYBERSONICS, INC. |
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