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

Diacore

K Number: K253926 · Decision Apr 10, 2026
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
161
Applicant Total
11
Review Days
123

Basic Information

Device Name
Diacore
K Number
K253926
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ShenB Co., Ltd.
Date Received
December 8, 2025
Decision Date
April 10, 2026
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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