510(k) K063355 ยท MPB Catheter, Hemodialysis, Non-Implanted
D-LINE CATHETER ST, DOUBLE LUMEN ST; EXTRA FLOW
| Applicant | Novosci Corp., The Woodlands TX, US |
| Decision | Unknown, Jul 27, 2007 |
| Received | Nov 7, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063355
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.