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Z1 CPAP SYSTEM

K140929 Class II Traditional
Decision Date
2014-10-17
Sponsor / Applicant
Human Design Medical, LLC

Technical Specification

510(k) Submission ID K140929
Product Code BZD
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5905
Decision Date 2014-10-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Z1 CPAP SYSTEM received FDA 510(k) clearance under submission number K140929, sponsored by Human Design Medical, 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 2014-10-17.

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.