510(k) K071202 ยท MSD Catheter, Hemodialysis, Implanted
DERMAPORT PERCUTANEOUS VASCULAR ACCESS SYSTEM (PVAS)
| Applicant | Dermaport, Inc., Stoughton WI, US |
| Decision | Unknown, Nov 30, 2007 |
| Received | May 1, 2007 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K071202
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.