510(k) K853903 ยท HHR Laser, Surgical, Gynecologic
ENDO-LASE CD40 CO2 FOR GYNECOLOGY
| Applicant | Endo Lase, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Feb 21, 1986 |
| Received | Sep 20, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853903
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.