meddevicedb.com FDA Device Reference

OptiPillows EPAP Mask

K181219 Class I Traditional
Decision Date
2018-08-03
Sponsor / Applicant
Cpapnea Medical Supply

Technical Specification

510(k) Submission ID K181219
Product Code LWF
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3900
Decision Date 2018-08-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OptiPillows EPAP Mask received FDA 510(k) clearance under submission number K181219, sponsored by Cpapnea Medical Supply. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2018-08-03.

Classification & Regulation

This clearance is catalogued under FDA product code LWF and 21 CFR 874.3900, within the Ear, Nose, Throat review panel as a Class I device.