510(k) K896630 ยท KAM Cannula, Sinus
SINOVENT MAXILLARY SINUS DRAINAGE SYSTEM
| Applicant | Atos Medical AB, Potomac MD, US |
| Decision | Substantially Equivalent, Jun 6, 1990 |
| Received | Nov 22, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896630
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.