510(k) K960742 ยท ETD Tube, Tympanostomy
TYMPANOSTOMY VENTILATION TUBE
| Applicant | Advanced Microbotics Corp., Portland OR, US |
| Decision | Substantially Equivalent, Apr 3, 1996 |
| Received | Feb 23, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960742
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.