510(k) K260716

Device
Neowise
Applicant
Cefla S.C.
510(k) number
K260716
Product code
LLZ
Decision
Substantially Equivalent (SESE)
Decision date
2026-05-04
Date received
2026-03-05
Regulation
892.2050
Classification name
System, Image Processing, Radiological
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Ilenia Muccione
Address
Via Selice Provinciale 23/A Imola (Bo) IT 40026 40026

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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