510(k) K812459 ยท ETD Tube, Tympanostomy
EXMOOR AURAL GROMMET AG/TI
| Applicant | Exmoor Plastics , Ltd., Walker MI, US |
| Decision | Substantially Equivalent, Sep 25, 1981 |
| Received | Aug 31, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812459
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.