510(k) K112188 ยท DZI Drill, Bone, Powered
PIEZOTOME SOLO
| Applicant | Satelec - Acteon, Inc., Mt. Laurel NJ, US |
| Decision | Substantially Equivalent, Feb 3, 2012 |
| Received | Jul 29, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112188
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.