510(k) K972099 ยท GEX Powered Laser Surgical Instrument
SHARPLAN EPITOUCH RUBY LASER SYSTEM
| Applicant | Sharplan Lasers, Inc., Warwick RI, US |
| Decision | Substantially Equivalent, Aug 27, 1997 |
| Received | Jun 4, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972099
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.