FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Electromagnetic Stimulation Systems

K Number: K232409 · Decision Apr 10, 2024
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
161
Applicant Total
14
Review Days
244

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Basic Information

Device Name
Electromagnetic Stimulation Systems
K Number
K232409
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shanghai Apolo Medical Technology Co., Ltd.
Date Received
August 10, 2023
Decision Date
April 10, 2024
Product Code
NGX
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
NGX Stimulator, Muscle, Powered, For Muscle Conditioning

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