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

NuEra Tight RF Family

K Number: K223856 · Decision Aug 11, 2023
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
14
Review Days
231

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Basic Information

Device Name
NuEra Tight RF Family
K Number
K223856
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bios S.R.L.
Date Received
December 23, 2022
Decision Date
August 11, 2023
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEI), 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
K223907 NuEra Tight RF Model APMD145.M70-US
K210867 NuEra Tight RF, NuEra Tight RF Plus
K201239 NuEra Tight Family, EMS Model
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. →