meddevicedb.com FDA Device Reference

DELTAWAVE Nasal Pillows System

K233415 Class II Traditional
Decision Date
2024-07-02
Sponsor / Applicant
Remsleep Holdings

Technical Specification

510(k) Submission ID K233415
Product Code BZD
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5905
Decision Date 2024-07-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DELTAWAVE Nasal Pillows System received FDA 510(k) clearance under submission number K233415, sponsored by Remsleep Holdings. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2024-07-02.

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.