510(k) K860063 ยท LNK Laser For Gastro-Urology Use
ND:YAG LASER SINGLE USE FIBER DELIVERY SYSTEM
| Applicant | Laser Media, Hauppauge NY, US |
| Decision | Substantially Equivalent, Feb 5, 1986 |
| Received | Jan 6, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860063
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.