510(k) K110503

AIRSTRIP REMOTE PATIENT MONITORING (RPM) by Airstrip Technologies, LP — Product Code MWI

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 10, 2011
Date Received
February 22, 2011
Clearance Type
Special
Expedited Review
No
Third Party Review
Yes

Device Classification

Device Name
Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Device Class
Class II
Regulation Number
870.2300
Review Panel
CV
Submission Type