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

StarFormer, TightWave

K Number: K221274 · Decision Sep 29, 2023
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
16
Review Days
515

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Basic Information

Device Name
StarFormer, TightWave
K Number
K221274
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fotona D.O.O.
Date Received
May 2, 2022
Decision Date
September 29, 2023
Product Code
IPF
Advisory Committee
Physical Medicine
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
IPF Stimulator, Muscle, Powered

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Other Clearances by Fotona D.O.O.

K Number Device Name
K241785 StarFormer (M008-3T)
K242202 LightWalker Laser System Family
K234061 StarFormer
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. →