FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Triangle System

K Number: K183319 · Decision May 10, 2019
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
296
Applicant Total
19
Review Days
161

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Basic Information

Device Name
Triangle System
K Number
K183319
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2920
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
AliveCor, Inc.
Date Received
November 30, 2018
Decision Date
May 10, 2019
Product Code
DXH
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DXH Transmitters And Receivers, Electrocardiograph, Telephone

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K210753 KardiaMobile 6L
K201985 KardiaAI
K191406 KardiaMobile, KardiaStation
K182396 KardiaMobile, KardiaStation
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