510(k) K925395 ยท LNK Laser For Gastro-Urology Use
TECHNOMED PULSOLITH 4000 LASER SYSTEM
| Applicant | Teknomed, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, May 21, 1993 |
| Received | Oct 26, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925395
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.