510(k) K884628 ยท DQR Cannula, Catheter
HARBORIN CENTRAL VENOUS CATHETER
| Applicant | Harbor Medical Devices, Inc., Boston MA, US |
| Decision | Substantially Equivalent, May 15, 1989 |
| Received | Nov 7, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884628
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.