510(k) K982333 ยท MSD Catheter, Hemodialysis, Implanted
MODIFICATION TO ULDALL DOUBLE LUMEN HEMODIALYSIS CATHETER SET AND TRAY
| Applicant | Cook, Inc., Bloomington IN, US |
| Decision | Substantially Equivalent, Feb 12, 1999 |
| Received | Jul 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982333
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.