FDA 510(k) FDA class 2 Substantially Equivalent 🇪🇸 Spain

Symmed Elite Aesthetic

K Number: K230412 · Decision Apr 13, 2023
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
77
Applicant Total
5
Review Days
57

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Basic Information

Device Name
Symmed Elite Aesthetic
K Number
K230412
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
Termosalud
Date Received
February 15, 2023
Decision Date
April 13, 2023
Product Code
PBX
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
PBX Massager, Vacuum, Radio Frequency Induced Heat

Similar 510(k) Clearances

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

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Other Clearances by Termosalud

K Number Device Name
K243488 VMAT PRO
K241656 Eneka Selectif
K230659 Zionic Aesthetic
K223680 Eneka Pro