FDA 510(k) Applications Submitted by MICHELLE DEETON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K990947 | 03/22/1999 | MODIFIED VERSAPULSE SELECT SINGLE WAVELENGTH, HO: YAG AND DUAL WAVELENGTH, HO: YAG/ND: YAG SURGICAL LASERS AND DELIVERY | LUMENIS, INC. |
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