FDA 510(k) Application Details - K153275

Device Classification Name Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

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510(K) Number K153275
Device Name Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Applicant Intelesens, Ltd.
17 Heron Road
Belfast BT3 9LE GB
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Contact Patricia Pepper
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Regulation Number 870.1025

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Classification Product Code MHX
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Date Received 11/12/2015
Decision Date 02/26/2016
Decision SESE - SUBST EQUIV
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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