510(k) K880503 ยท FFK Lithotriptor, Electro-Hydraulic
MDL-1 LASERTRIPTER
| Applicant | Candela Laser Corp., Wayland MA, US |
| Decision | Substantially Equivalent, Jun 17, 1988 |
| Received | Feb 8, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880503
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.