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

Empatica Health Monitoring Platform

K Number: K221282 · Decision Nov 20, 2022
Classifications
1
FEI Numbers
400
Registration Numbers
400
Same Product Code
725
Applicant Total
8
Review Days
201

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Basic Information

Device Name
Empatica Health Monitoring Platform
K Number
K221282
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Empatica S.r.l.
Date Received
May 3, 2022
Decision Date
November 20, 2022
Product Code
DQA
Advisory Committee
Cardiovascular
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
DQA Oximeter

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DQA), 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
K181861 Embrace
K172935 Embrace