meddevicedb.com FDA Device Reference

PATI (Protector Against Tongue Injury)

K221469 Class II Traditional
Decision Date
2023-02-22
Sponsor / Applicant
Neurovice, LLC

Technical Specification

510(k) Submission ID K221469
Product Code JXL
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5070
Decision Date 2023-02-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PATI (Protector Against Tongue Injury) received FDA 510(k) clearance under submission number K221469, sponsored by Neurovice, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2023-02-22.

Classification & Regulation

This clearance is catalogued under FDA product code JXL and 21 CFR 882.5070, within the Neurology review panel as a Class II device.