510(k) K103595 ยท ETD Tube, Tympanostomy
ACCLARENT TYMPANOSTOMY TUBE AND TYMPANOSTOMY TUBE DELIVERY SYSTEM
| Applicant | Acclarent, Inc., Rmenlo Park CA, US |
| Decision | Substantially Equivalent, Apr 1, 2011 |
| Received | Dec 8, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103595
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.