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FDA 510(k), K123229, REMOTE PRESENCE SYSTEM, MODEL RP-VITA
FDA 510(k), K123229, REMOTE PRESENCE SYSTEM, MODEL RP-VITA
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510(K) Number: K123229
Device Name: REMOTE PRESENCE SYSTEM, MODEL RP-VITA
Manufacturer: INTOUCH HEALTH, INC.
Device Classification Name: transmitters and receivers, physiological signal, radiofrequency
Regulation Number: 870.2910
Classification Product Code: DRG
Date Received: 10/15/2012
Decision Date: 11/20/2012
Regulation Medical Specialty: Cardiovascular
Device Name: REMOTE PRESENCE SYSTEM, MODEL RP-VITA
Manufacturer: INTOUCH HEALTH, INC.
Device Classification Name: transmitters and receivers, physiological signal, radiofrequency
Regulation Number: 870.2910
Classification Product Code: DRG
Date Received: 10/15/2012
Decision Date: 11/20/2012
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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