FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

Embrace

K Number: K172935 · Decision Jan 26, 2018
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
9
Applicant Total
8
Review Days
122

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Basic Information

Device Name
Embrace
K Number
K172935
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1580
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Empatica S.r.l.
Date Received
September 26, 2017
Decision Date
January 26, 2018
Product Code
POS
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
POS Physiological Signal Based Seizure Monitoring System

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (POS), ordered by most recent decision date.

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Other Clearances by Empatica S.r.l.

K Number Device Name
K252981 EmbraceMini
K250515 EpiMonitor
K242737 Empatica Health Monitoring Platform; EmbracePlus; Empatica Care; Care Portal
K232915 EpiMonitor
K230457 Empatica Health Monitoring Platform; EmbracePlus; Empatica Care; Care Portal
K221282 Empatica Health Monitoring Platform
K181861 Embrace