510(k) K810703 ยท ETD Tube, Tympanostomy
EXMOOR AURAL GROMMET AG/T2
| Applicant | Exmoor Plastics , Ltd., Walker MI, US |
| Decision | Substantially Equivalent, Apr 14, 1981 |
| Received | Mar 16, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810703
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.