510(k) K011916 ยท MSD Catheter, Hemodialysis, Implanted
SUPER C HEMODIALYSIS/APHERESIS CHRONIC CATHETER, MODEL DC-36 SERIES, DC-40 SERIES, DC-45 SERIES
| Applicant | Horizon Medical Products, Inc., Manchester GA, US |
| Decision | Substantially Equivalent, Oct 31, 2001 |
| Received | Jun 20, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011916
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.