FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

OptiLUV Device

K Number: K250734 · Decision Sep 10, 2025
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
77
Applicant Total
18
Review Days
183

Basic Information

Device Name
OptiLUV Device
K Number
K250734
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
Pollogen, Ltd.
Date Received
March 11, 2025
Decision Date
September 10, 2025
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

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