510(k) K042016 ยท MSD Catheter, Hemodialysis, Implanted
DATASCOPE PROGUIDE CHRONIC DIALYSIS CATHETER
| Applicant | Datascope Corp., Manwah NJ, US |
| Decision | Substantially Equivalent, Sep 23, 2004 |
| Received | Jul 27, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042016
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.