Medical Device Manufacturer · BE , Gent-Zwijnaarde

Feops NV - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 2021
4
Total
3
Cleared
1
Denied
FDA 510(k) Regulatory Record - Feops NV Cardiovascular ✕
3 devices
1-3 of 3
Cleared Nov 25, 2025
FEops HEARTguide Simulation Application
K250635 · QQI
Cardiovascular · 267d
Cleared Feb 25, 2022
FEops HEARTguide
K214066 · QQI
Cardiovascular · 60d
Not Cleared Sep 08, 2021
FEops HEARTguide
DEN200030 · QQI
Cardiovascular · 489d
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All4 Cardiovascular 3 Radiology 1