510(k) K130320 ยท DQA Oximeter
BEDSIDE RESPIRATORY PATIENT MONITORING SYSTEM, BEDSIDE RESPIRATORY PATIENT MONITORING SYSTEM WITH RESPIRATION RATE SOFTW
| Applicant | Covidien, Boulder CO, US |
| Decision | Substantially Equivalent, Feb 4, 2014 |
| Received | Feb 8, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130320
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.