510(k) K880071 ยท FCS Light, Catheter, Fiberoptic, Glass, Ureteral
SURGI-LIGHT ND:YAG LASER FOR UROLOGICAL USE
| Applicant | Laserguide, Santa Barbara CA, US |
| Decision | Substantially Equivalent, Mar 22, 1988 |
| Received | Jan 11, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880071
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.