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

EM25 - glute toning device

K Number: K143737 · Decision Jul 27, 2015
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
161
Applicant Total
18
Review Days
209

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Basic Information

Device Name
EM25 - glute toning device
K Number
K143737
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hivox Biotek, Inc.
Date Received
December 30, 2014
Decision Date
July 27, 2015
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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Other Clearances by Hivox Biotek, Inc.

K Number Device Name
K260425 TENS / EMS DEVICE (FT-247 Series) (FT-247, FT-237)
K242815 POCKET TENS (EP-300)
K232675 Heating Tens, FT-615
K223308 HEATING TENS/EMS, FT-810R
K221384 Heating TENS/EMS Device, FT-240-1, Heating TENS/EMS Device, FT-240-2
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
Search all 18 clearances from Hivox Biotek, Inc. →