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

GEMS-H

K Number: K213452 · Decision Apr 21, 2022
Classifications
1
FEI Numbers
8
Registration Numbers
8
Same Product Code
23
Applicant Total
40
Review Days
177

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Basic Information

Device Name
GEMS-H
K Number
K213452
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3480
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Samsung Electronics Co., Ltd.
Date Received
October 26, 2021
Decision Date
April 21, 2022
Product Code
PHL
Advisory Committee
Physical Medicine
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
PHL Powered Exoskeleton

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