meddevicedb.com FDA Device Reference

ManaSport

K210284 Class II Traditional
Decision Date
2022-04-26
Sponsor / Applicant
Manamed, Inc.

Technical Specification

510(k) Submission ID K210284
Product Code IMI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5300
Decision Date 2022-04-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ManaSport received FDA 510(k) clearance under submission number K210284, sponsored by Manamed, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2022-04-26.

Classification & Regulation

This clearance is catalogued under FDA product code IMI and 21 CFR 890.5300, within the Physical Medicine review panel as a Class II device.