510(k) K972057 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
POWERTREK INSTRUMENTS
| Applicant | Medtrek Corp., Branford CT, US |
| Decision | Substantially Equivalent, Nov 5, 1997 |
| Received | Jun 2, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972057
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.