510(k) K061450 ยท DQE Catheter, Oximeter, Fiber-Optic
HOSPIRA LATEX-FREE ADVANCED SENSOR CATHETERS; HOSPIRA LATEX-FREE CRITICAL CARE CATHETERS
| Applicant | Hospira, Inc., Lake Forest IL, US |
| Decision | Substantially Equivalent, Aug 4, 2006 |
| Received | May 25, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061450
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.