FDA 510(k) Applications Submitted by SHARPLIGHT TECHNOLOGIES LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K111303 | 05/09/2011 | DERMATOLOGICAL TREATMENT DEVICE FAMILY | SHARPLIGHT TECHNOLOGIES LTD. |
| K082876 | 09/29/2008 | BEAMAX/ FORMAX PULSED LIGHT DEVICE FAMILY | SHARPLIGHT TECHNOLOGIES LTD. |
| K173169 | 09/29/2017 | Rapid Family | SharpLight Technologies Ltd. |
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