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

TENSCARE ULTIMA NMS/EMS

K Number: K023997 · Decision Mar 3, 2003
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
13
Review Days
90

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Basic Information

Device Name
TENSCARE ULTIMA NMS/EMS
K Number
K023997
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tenscare, Ltd.
Date Received
December 3, 2002
Decision Date
March 3, 2003
Product Code
IPF
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
IPF Stimulator, Muscle, Powered

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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)
K200694 Perfect EMS
K191312 Perfect PFE
K142506 TensCare KegelFit
K103698 TENSCARE ITOUCH SURE MODEL ITS
K082377 TENSCARE ITOUCH MODEL(S) EASY AND PLUS
K020846 ULTIMA TENS XL-A1
Search all 13 clearances from Tenscare, Ltd. →