510(k) K953802 ยท ETD Tube, Tympanostomy
TYMPANOSTOMY TUBE
| Applicant | Bluff City Medical Technologies, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Oct 24, 1995 |
| Received | Aug 7, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953802
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.