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

Pain Therapy System, Model PTS-II

K Number: K150277 · Decision Feb 12, 2016
Classifications
1
FEI Numbers
160
Registration Numbers
160
Same Product Code
227
Applicant Total
4
Review Days
372

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Basic Information

Device Name
Pain Therapy System, Model PTS-II
K Number
K150277
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Counter Scientific Development (Gz), Ltd.
Date Received
February 5, 2015
Decision Date
February 12, 2016
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 Counter Scientific Development (Gz), Ltd.

K Number Device Name
K161537 OTC TENS Device, Model PTS-IV
K151279 Counter OTC TENS Device, Model CSD-737Z
K132993 COUNTER OTC TENS DEVICE