510(k) K901723 ยท LNK Laser For Gastro-Urology Use
MDL-2000 LASERTRIPTER
| Applicant | Candela Laser Corp., Wayland MA, US |
| Decision | Substantially Equivalent, Jul 13, 1990 |
| Received | Apr 16, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901723
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.