510(k) K061159 ยท DQE Catheter, Oximeter, Fiber-Optic
OPTICATH CENTRAL VENOUS OXIMETRY PROBE WITH FLUIDIC SEAL WITH/WITHOUT HEPARIN
| Applicant | Hospira, Inc., Lake Forest IL, US |
| Decision | Substantially Equivalent, Jun 26, 2006 |
| Received | Apr 26, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061159
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.