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

CardiMax Electrocardiograph

K Number: K173226 · Decision Apr 16, 2018
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
68
Review Days
195

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Basic Information

Device Name
CardiMax Electrocardiograph
K Number
K173226
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fukuda Denshi USA, Inc.
Date Received
October 3, 2017
Decision Date
April 16, 2018
Product Code
DPS
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
DPS Electrocardiograph

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