510(k) K121871 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, Jul 3, 2012 |
| Received | Jun 27, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121871
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.