510(k) K974164 ยท FFK Lithotriptor, Electro-Hydraulic
SWISS LITHOCLAST MASTER HANDPIECE AND 3.2 MM PROBE
| Applicant | Medical Device Consultants, Inc., North Attleboro MA, US |
| Decision | Substantially Equivalent, Dec 18, 1997 |
| Received | Nov 5, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974164
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.