510(k) K980517 ยท GEX Powered Laser Surgical Instrument
EPILASER NORMAL MODE RUBY LASER
| Applicant | Palomar Medical Products, Inc., Raleigh NC, US |
| Decision | Substantially Equivalent, Jul 21, 1998 |
| Received | Feb 10, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980517
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.