FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

NEUROTECH KNEEHAB

K Number: K024258 · Decision Mar 4, 2005
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
32
Review Days
802

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Basic Information

Device Name
NEUROTECH KNEEHAB
K Number
K024258
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bio-Medical Research, Ltd.
Date Received
December 23, 2002
Decision Date
March 4, 2005
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 Bio-Medical Research, Ltd.

K Number Device Name
K203513 SLENDERTONE Evolve Abs, Type 735
DEN170049 Innovo
K180688 SLENDERTONE CoreFit Abs 8, Type 734
K161974 SLENDERTONE® Connect Abs, Type 570
K151903 Slendertone connect Abs
K112934 NEUROTECH RECOVERY
K112258 NEUROTECH PLUS
K103031 BMR FACE
K110350 KNEEHAB XP
K102614 AVIVAFIX CONDUCTIVE GARMENT-KNEE/SHOULDER/UPPER BACK, TYPE 40
Search all 32 clearances from Bio-Medical Research, Ltd. →