510(k) K031988 ยท GEX Powered Laser Surgical Instrument
AURORA DS
| Applicant | Syneron Medical, Ltd., Yoqneam Illit, IL |
| Decision | Substantially Equivalent, Aug 1, 2003 |
| Received | Jun 27, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031988
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.