meddevicedb.com FDA Device Reference

AquaCast Mask

K252174 Class II Traditional
Decision Date
2025-09-03
Sponsor / Applicant
Blessing Cathay Corporation

Technical Specification

510(k) Submission ID K252174
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2025-09-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AquaCast Mask received FDA 510(k) clearance under submission number K252174, sponsored by Blessing Cathay Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2025-09-03.

Classification & Regulation

This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.