meddevicedb.com FDA Device Reference

MR Egometer Pedal, MR Ergometer Push/Pull, MR Ergometer Up/Down, MR Ergometer Dorsal Ankle Flex, MR Ergometer Pedal Ultra

K202979 Class II Abbreviated
Decision Date
2020-12-21
Sponsor / Applicant
Lode B.V.

Technical Specification

510(k) Submission ID K202979
Product Code ISD
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5360
Decision Date 2020-12-21
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MR Egometer Pedal, MR Ergometer Push/Pull, MR Ergometer Up/Down, MR Ergometer Dorsal Ankle Flex, MR Ergometer Pedal Ultra received FDA 510(k) clearance under submission number K202979, sponsored by Lode B.V.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2020-12-21.

Classification & Regulation

This clearance is catalogued under FDA product code ISD and 21 CFR 890.5360, within the Physical Medicine review panel as a Class II device.