510(k) K022000 ยท MSD Catheter, Hemodialysis, Implanted
POURCHEZ RETRO TWIN LUMEN CHRONIC HEMODIALYSIS CATHETER WITH SEPARATED TIPS (WITH AND WITHOUT SIDE HOLES)
| Applicant | Spire Biomedical, Inc., Bedford MA, US |
| Decision | Substantially Equivalent, Jul 19, 2002 |
| Received | Jun 19, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K022000
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.