510(k) K853904 ยท GEX Powered Laser Surgical Instrument
ENDO-LASE CD40 FOR UROLOGY
| Applicant | Endo Lase, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Oct 25, 1985 |
| Received | Sep 20, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853904
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.