510(k) K111303 ยท GEX Powered Laser Surgical Instrument
DERMATOLOGICAL TREATMENT DEVICE FAMILY
| Applicant | Sharplight Technologies, Ltd., Zichron Yaacov, IL |
| Decision | Substantially Equivalent, Dec 21, 2011 |
| Received | May 9, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111303
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.