510(k) K110503 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
AIRSTRIP REMOTE PATIENT MONITORING (RPM)
| Applicant | Airstrip Technologies, LP, San Antonio TX, US |
| Decision | Substantially Equivalent, Mar 10, 2011 |
| Received | Feb 22, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110503
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.