510(k) K950819 ยท GEX Powered Laser Surgical Instrument
SLT SIDEFIRING REFRACTIVE FIBER (HIGH POWER DENSITY FIBER)
| Applicant | Surgical Laser Technologies, Inc., Oaks PA, US |
| Decision | Substantially Equivalent, Apr 18, 1995 |
| Received | Feb 23, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950819
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.