510(k) K060288 ยท MSD Catheter, Hemodialysis, Implanted
RETRO SILVER AND XPRESSO SILVER CHRONIC HEMODIALYSIS CATHETERS
| Applicant | Spire Biomedical, Inc., Bedford MA, US |
| Decision | Unknown, Sep 1, 2006 |
| Received | Feb 6, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060288
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.