meddevicedb.com FDA Device Reference

DeVilbiss DV6WM Wireless Modem

K152810 Class II Traditional
Decision Date
2016-01-21
Sponsor / Applicant
Devilbiss Healthcare, LLC

Technical Specification

510(k) Submission ID K152810
Product Code BZD
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5905
Decision Date 2016-01-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DeVilbiss DV6WM Wireless Modem received FDA 510(k) clearance under submission number K152810, sponsored by Devilbiss Healthcare, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2016-01-21.

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.