510(k) K122223 ยท BZQ Monitor, Breathing Frequency
NEW: INTELLIVUE CL RESPIRATION POD NEW: SPECIALIZED ASSESSORY: MOBILE CL RESP ATTACHMENT MODIFIED: INTELLIVUE PATIENT MO
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Boeblingen, DE |
| Decision | Substantially Equivalent, Apr 12, 2013 |
| Received | Jul 25, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122223
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.