meddevicedb.com FDA Device Reference

Nice1

K143197 Class II Traditional
Decision Date
2014-12-23
Sponsor / Applicant
Nice Recovery Systems, LLC

Technical Specification

510(k) Submission ID K143197
Product Code IRP
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5650
Decision Date 2014-12-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Nice1 received FDA 510(k) clearance under submission number K143197, sponsored by Nice Recovery Systems, 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 2014-12-23.

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.