FEops HEARTguide— 510(k) DEN200030

Unknown

Feops NV

FDA 510(k) clearance DEN200030 for FEops HEARTguide, Unknown on 2021-09-08. Applicant: Feops NV.

Clearance details

Applicant: Feops NV
Product code: Code QQI
Advisory panel: Cardiovascular
Date received: 2020-05-07
Decision date: 2021-09-08
Decision: Unknown
Clearance type: Direct
Location: Gent-Zwijnaarde, BE

View on FDA.gov ↗

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