NemoScan— 510(k) K232698

Substantially Equivalent

Software Nemotec S.L.

FDA 510(k) clearance K232698 for NemoScan, Substantially Equivalent on 2024-01-18. Applicant: Software Nemotec S.L.. Device class: 2.

Clearance details

Applicant: Software Nemotec S.L.
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2023-09-05
Decision date: 2024-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Leganes, ES

Download summary PDF View on FDA.gov ↗

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