510(k) K022644 ยท NFK Kit, Repair, Catheter, Hemodialysis
RETRO REPAIR KIT, MODEL PRRK5
| Applicant | Spire Biomedical, Inc., Bedford MA, US |
| Decision | Unknown, Nov 6, 2002 |
| Received | Aug 8, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022644
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.