FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇪 Sweden

The IQoolTM Warm System

K Number: K180375 · Decision May 18, 2018
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
157
Applicant Total
4
Review Days
95

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Basic Information

Device Name
The IQoolTM Warm System
K Number
K180375
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5900
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Braincool AB
Date Received
February 12, 2018
Decision Date
May 18, 2018
Product Code
DWJ
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
DWJ System, Thermal Regulating

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Other Clearances by Braincool AB

K Number Device Name
K232844 The IQoolTM System
DEN210027 The Cooral System
K162523 The IQool System