510(k) K023023 ยท MSD Catheter, Hemodialysis, Implanted
LIFESITE HEMODIALYSIS ACCESS SYSTEM, CANNULA EXCHANGE KIT, INSERTION KIT, ACCESS CANNILA
| Applicant | Vasca, Inc., Tewksburt MA, US |
| Decision | Substantially Equivalent, Dec 4, 2003 |
| Received | Sep 11, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023023
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.