FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

NuEra Tight Family, EMS Model

K Number: K201239 · Decision Dec 31, 2020
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
161
Applicant Total
14
Review Days
238

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Basic Information

Device Name
NuEra Tight Family, EMS Model
K Number
K201239
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bios S.R.L.
Date Received
May 7, 2020
Decision Date
December 31, 2020
Product Code
NGX
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
NGX Stimulator, Muscle, Powered, For Muscle Conditioning

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NGX), ordered by most recent decision date.

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Other Clearances by Bios S.R.L.

K Number Device Name
K243445 Splendor X (Alex, Alex2, Nd:YAG, Alex+Nd:YAG)
K241407 Splendor X (Alex, Alex2, Nd:YAG, Alex+Nd:YAG)
K230755 NuEra Tight RF Model OptiStream
K223856 NuEra Tight RF Family
K223907 NuEra Tight RF Model APMD145.M70-US
K210867 NuEra Tight RF, NuEra Tight RF Plus
K200359 NuEra Tight, NuEra Tight EMS
K161632 FAMILY OF SQUARE EPIL (Alex, Alex2, Nd:Yag, Alex+Nd:Yag)
K153229 Superbium
K151296 Family of Radiofrequency System (Biorevital RF MED, ThermiSmooth 250)
Search all 14 clearances from Bios S.R.L. →