510(k) K874618 ยท DQR Cannula, Catheter
BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER
| Applicant | Bentley Laboratories, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 19, 1988 |
| Received | Nov 9, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874618
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.