510(k) K080722 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
PRIMADO SURGICAL DRILL
| Applicant | Nakanishi, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Sep 17, 2008 |
| Received | Mar 13, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080722
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.