Sonio Suspect— 510(k) K243614

Substantially Equivalent

Sonio

FDA 510(k) clearance K243614 for Sonio Suspect, Substantially Equivalent on 2025-02-21. Applicant: Sonio. Device class: 2.

Clearance details

Applicant
Sonio
Product code
Code POK
Device class
Class 2
Regulation
21 CFR 892.2060
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Paris, FR
Download summary PDFView on FDA.gov ↗

Recent devices under product code POK

view all

More clearances from Sonio

view all

Data sourced from openFDA. This site is unofficial and independent of the FDA.