510(k) K931779 ยท FFK Lithotriptor, Electro-Hydraulic
EHL PULSE GENERATOR
| Applicant | Psi Medical Products, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Feb 15, 1994 |
| Received | Apr 9, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931779
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.