510(k) K895178 ยท FFK Lithotriptor, Electro-Hydraulic
TECHNOMED PULSOLITH LASER SYSTEM
| Applicant | Teknomed, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Oct 6, 1989 |
| Received | Aug 10, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895178
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.