510(k) K232966

Device
FISIOWARM 7.0
Applicant
Golden Star Srl
510(k) number
K232966
Product code
PBX
Decision
Substantially Equivalent (SESE)
Decision date
2024-12-26
Date received
2023-09-21
Regulation
878.4400
Classification name
Massager, Vacuum, Radio Frequency Induced Heat
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Tiziaria Borrelli
Address
Via Enrico Pallini 9 Roma IT 00149 00149

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code PBX#

510(k), Device, Applicant table
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