meddevicedb.com FDA Device Reference

FEops HEARTguide

DEN200030 Class II Direct
Decision Date
2021-09-08
Sponsor / Applicant
Feops NV

Technical Specification

510(k) Submission ID DEN200030
Product Code QQI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1405
Decision Date 2021-09-08
Clearance Pathway Direct

Official Documentation

No FDA summary/statement PDF is linked for this clearance in the current dataset. Consult the product code and regulation citation above to locate predicate documentation.

Clearance Summary

FEops HEARTguide received FDA 510(k) clearance under submission number DEN200030, sponsored by Feops NV. The device was reviewed via the Direct premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2021-09-08.

Classification & Regulation

This clearance is catalogued under FDA product code QQI and 21 CFR 870.1405, within the Cardiovascular review panel as a Class II device.