FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

Perfect EMS

K Number: K200694 · Decision Jun 4, 2021
Classifications
1
FEI Numbers
160
Registration Numbers
160
Same Product Code
227
Applicant Total
13
Review Days
444

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Basic Information

Device Name
Perfect EMS
K Number
K200694
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tenscare, Ltd.
Date Received
March 17, 2020
Decision Date
June 4, 2021
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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Other Clearances by Tenscare, Ltd.

K Number Device Name
K232441 Unipro (K-UNIPRO-US)
K230926 Ova+ (K-OVAP-USA)
K230983 Unicare (K-UNICARE-USA)
K231053 Unicare (K-UNICARE-USA)
K191312 Perfect PFE
K142506 TensCare KegelFit
K103698 TENSCARE ITOUCH SURE MODEL ITS
K082377 TENSCARE ITOUCH MODEL(S) EASY AND PLUS
K023997 TENSCARE ULTIMA NMS/EMS
K020846 ULTIMA TENS XL-A1
Search all 13 clearances from Tenscare, Ltd. →