FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

TENS / EMS DEVICE (FT-247 Series) (FT-247, FT-237)

K Number: K260425 · Decision Jun 16, 2026
Classifications
1
FEI Numbers
160
Registration Numbers
160
Same Product Code
227
Applicant Total
18
Review Days
126

Basic Information

Device Name
TENS / EMS DEVICE (FT-247 Series) (FT-247, FT-237)
K Number
K260425
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hivox Biotek, Inc.
Date Received
February 10, 2026
Decision Date
June 16, 2026
Product Code
NUH
Advisory Committee
Neurology
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
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter

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K Number Device Name
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K211403 HIVOX OTC Electrical Stimulator, FT610-B
K203574 HIVOX OTC Electrical Stimulator, EM59-l, HIVOX OTC Electrical Stimulator, EM59-2
K192264 HIVOX Spopad EMS SP-911, SP-921
K190347 HIVOX OTC Electrical Stimulator
K171803 HIVOX OTC Electrical Stimulator
K143737 EM25 - glute toning device
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