510(k) K881884 ยท DQR Cannula, Catheter
HARBOR CENTRAL VENOUS CATHETER
| Applicant | Harbor Medical Devices, Inc., Boston MA, US |
| Decision | Substantially Equivalent, Jul 28, 1988 |
| Received | May 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881884
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.