510(k) K133921 ยท ETD Tube, Tympanostomy
PRECEPTIS TYMPANOSTOMY TUBE INSERTER
| Applicant | Preceptis Medical, Plymouth MN, US |
| Decision | Substantially Equivalent, Aug 22, 2014 |
| Received | Dec 23, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133921
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.