510(k) K091760 ยท MSD Catheter, Hemodialysis, Implanted
DERMAPORT PORTED VASCULAR ACCESS SYSTEM (PVAS)
| Applicant | Dermaport, Inc., Santa Clarita CA, US |
| Decision | Substantially Equivalent, Jul 20, 2009 |
| Received | Jun 16, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K091760
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.