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

Low-frequency Multi-function physiotherapy instrument

K Number: K172837 · Decision Nov 26, 2018
Classifications
1
FEI Numbers
160
Registration Numbers
160
Same Product Code
227
Applicant Total
5
Review Days
433

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Basic Information

Device Name
Low-frequency Multi-function physiotherapy instrument
K Number
K172837
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shenzhen Osto Technology Co., Ltd.
Date Received
September 19, 2017
Decision Date
November 26, 2018
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NUH), ordered by most recent decision date.

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Other Clearances by Shenzhen Osto Technology Co., Ltd.

K Number Device Name
K212989 Low-frequency Stimulator (Model: AST-645, AST-646)
K182136 Intelligent Wireless Fitness Apparatus (Model: AST-301, AST-302, AST-303)
K172897 Neck Care Therapy, Model: SYK 509B
K172834 Dual output digital therapy massager