510(k) K233092

Device
Pain Therapy Device (SM9075, SM9910, SM9067, SM9587W)
Applicant
Chongqing Rob Linka Science and Technology Co., Ltd.
510(k) number
K233092
Product code
NUH
Decision
Substantially Equivalent (SESE)
Decision date
2024-02-12
Date received
2023-09-26
Regulation
882.5890
Classification name
Stimulator, Nerve, Transcutaneous, Over-The-Counter
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
Huirong Lu
Address
B3-2, Liangjiang Health Science And Technology City, # 2 Yuekang Rd., Fuxing St., Beibei District Chongqing CN 400700 400700

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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510(k), Device, Applicant table
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