FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇮 Slovenia

StarFormer (M008-3T)

K Number: K241785 · Decision Mar 27, 2025
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
5
Applicant Total
16
Review Days
280

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Basic Information

Device Name
StarFormer (M008-3T)
K Number
K241785
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fotona D.O.O.
Date Received
June 20, 2024
Decision Date
March 27, 2025
Product Code
QPL
Advisory Committee
Neurology
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
QPL Electromagnetic Stimulator, Pain Relief

Similar 510(k) Clearances

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

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Other Clearances by Fotona D.O.O.

K Number Device Name
K242202 LightWalker Laser System Family
K234061 StarFormer
K221274 StarFormer, TightWave
K223540 AvalancheLase Family
K221712 Fotona XPulse Laser System Family (XPulse 1064 nm, XPulse 810 nm, XPulse 980 nm)
K213267 Dynamis Pro Family
K202991 Fotona XPulse Pro Laser Platform
K202985 LightWalker Laser System Family
K202172 StarWalker
K193656 SkyPulse
Search all 16 clearances from Fotona D.O.O. →