510(k) K050957 ยท MDM Instrument, Manual, Surgical, General Use
EUTROCHAR
| Applicant | Special Devices, Inc., Grass Valley CA, US |
| Decision | Substantially Equivalent, May 18, 2005 |
| Received | Apr 15, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050957
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.