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FDA 510(k), K160862, AirStrip RPM
FDA 510(k), K160862, AirStrip RPM
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510(K) Number: K160862
Device Name: AirStrip RPM
Manufacturer: AirStrip Technologies, Inc.
Device Classification Name: system, network and communication, physiological monitors
Regulation Number: 870.2300
Classification Product Code: MSX
Date Received: 03/29/2016
Decision Date: 09/19/2016
Regulation Medical Specialty: Cardiovascular
Device Name: AirStrip RPM
Manufacturer: AirStrip Technologies, Inc.
Device Classification Name: system, network and communication, physiological monitors
Regulation Number: 870.2300
Classification Product Code: MSX
Date Received: 03/29/2016
Decision Date: 09/19/2016
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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