FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

CUBE Air Purifier

K Number: K211139 · Decision Nov 26, 2021
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
35
Applicant Total
40
Review Days
224

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Basic Information

Device Name
CUBE Air Purifier
K Number
K211139
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6500
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Samsung Electronics Co., Ltd.
Date Received
April 16, 2021
Decision Date
November 26, 2021
Product Code
FRA
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FRA Purifier, Air, Ultraviolet, Medical

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