meddevicedb.com FDA Device Reference

MOUTHPIECE BREATHING

K901563 Class II Traditional
Decision Date
1990-06-28
Sponsor / Applicant
Scott All-Sports, Inc.

Technical Specification

510(k) Submission ID K901563
Product Code JXL
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5070
Decision Date 1990-06-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MOUTHPIECE BREATHING received FDA 510(k) clearance under submission number K901563, sponsored by Scott All-Sports, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1990-06-28.

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.