510(k) K041523 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
XPS 3000 SYSTEM
| Applicant | Medtronic Xomed, Inc., Jacksonville FL, US |
| Decision | Substantially Equivalent, Jul 23, 2004 |
| Received | Jun 8, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041523
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.