510(k) K862456 ยท HHR Laser, Surgical, Gynecologic
ND:YAG LASER 4000/6000/8000 ENDOMETRIAL ABLATION
| Applicant | Cooper Lasersonics, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Aug 12, 1986 |
| Received | Jun 27, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862456
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.