meddevicedb.com FDA Device Reference

Endoscopy Oxygen Mask

K220533 Class II Traditional
Decision Date
2022-11-16
Sponsor / Applicant
Engineered Medical Systems, Inc.

Technical Specification

510(k) Submission ID K220533
Product Code CCK
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.1400
Decision Date 2022-11-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Endoscopy Oxygen Mask received FDA 510(k) clearance under submission number K220533, sponsored by Engineered Medical Systems, 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 2022-11-16.

Classification & Regulation

This clearance is catalogued under FDA product code CCK and 21 CFR 868.1400, within the Anesthesiology review panel as a Class II device.