510(k) K061646 ยท FBO Cystourethroscope
LASERSCOPE GUIDED DELIVERY DEVICE (GDD) CYSTOURETHROSCOPE & ACCESSORIES
| Applicant | Laserscope, San Jose CA, US |
| Decision | Substantially Equivalent, Jun 27, 2006 |
| Received | Jun 12, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061646
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.