510(k) K960821 ยท GEX Powered Laser Surgical Instrument
SLT FUMICH PROBE GUIDE
| Applicant | Surgical Laser Technologies, Inc., Oaks PA, US |
| Decision | Substantially Equivalent, May 16, 1996 |
| Received | Feb 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960821
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.