meddevicedb.com FDA Device Reference

ManaCold Compression System

K260944 Class II Traditional
Decision Date
2026-08-12
Sponsor / Applicant
Manamed, LLC

Technical Specification

510(k) Submission ID K260944
Product Code IRP
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5650
Decision Date 2026-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ManaCold Compression System received FDA 510(k) clearance under submission number K260944, sponsored by Manamed, LLC. 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 2026-08-12.

Classification & Regulation

This clearance is catalogued under FDA product code IRP and 21 CFR 890.5650, within the Physical Medicine review panel as a Class II device.