510(k) K880173 ยท HHR Laser, Surgical, Gynecologic
MODEL 4900 ND:YAG LASER FOR ENDOMETRIAL ABLATION
| Applicant | Cooper Lasersonics, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Mar 24, 1988 |
| Received | Jan 15, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880173
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.