510(k) K953993 ยท ETD Tube, Tympanostomy
TYMPASNOSTOMY TUBE
| Applicant | Hampton Precision Products, Inc., Fenton MO, US |
| Decision | Substantially Equivalent, Sep 12, 1995 |
| Received | Aug 24, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953993
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.