510(k) K924664 ยท GEX Powered Laser Surgical Instrument
SURGILASE FIBERLASE CO2 LASER WAVEGUIDE
| Applicant | Surgilase, Inc., Warwick RI, US |
| Decision | Substantially Equivalent, Apr 15, 1993 |
| Received | Sep 1, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924664
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.