510(k) K243716

Device
Zionic Pro Max (Radiofrequency)
Applicant
Termosalud S.L.
510(k) number
K243716
Product code
PBX
Decision
Substantially Equivalent (SESE)
Decision date
2025-05-28
Date received
2024-12-02
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
N

Applicant Contact#

Contact
Cristina Cifuentes
Address
Ataulfo Friera Tarfe 8 Gijon ES 33211 33211

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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