510(k) K062999 ยท DQE Catheter, Oximeter, Fiber-Optic
OPTICATH CENTRAL VENOUS OXIMETRY PROBE WITH SEAL WITH HEPARIN
| Applicant | Hospira, Inc., Lake Forest IL, US |
| Decision | Substantially Equivalent, Nov 3, 2006 |
| Received | Oct 2, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062999
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.