meddevicedb.com FDA Device Reference

Sleep Apnea Breathing Therapy Mask:JoyMask 20-B Full Face Mask, JoyMask 21-B Full Face Mask

K251920 Class II Traditional
Decision Date
2026-05-21
Sponsor / Applicant
Dcstar, Inc.

Technical Specification

510(k) Submission ID K251920
Product Code BZD
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5905
Decision Date 2026-05-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sleep Apnea Breathing Therapy Mask:JoyMask 20-B Full Face Mask, JoyMask 21-B Full Face Mask received FDA 510(k) clearance under submission number K251920, sponsored by Dcstar, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2026-05-21.

Classification & Regulation

This clearance is catalogued under FDA product code BZD and 21 CFR 868.5905, within the Anesthesiology review panel as a Class II device.