510(k) K112235 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING
| Applicant | Airstrip Technologies, LP, San Antonio TX, US |
| Decision | Substantially Equivalent, Aug 26, 2011 |
| Received | Aug 4, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112235
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.