510(k) K920865 ยท GEX Powered Laser Surgical Instrument
SHARPLAN 2100,3000,SHARPLASER 65, 40
| Applicant | Sharplan Lasers, Inc., Washington, D.C. DC, US |
| Decision | Substantially Equivalent, Aug 2, 1993 |
| Received | Feb 25, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920865
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.