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LUNA CPAP AND AUTO-CPAP SYSTEM

K141770 Class II Traditional
Decision Date
2015-04-22
Sponsor / Applicant
3B Medical, Inc.

Technical Specification

510(k) Submission ID K141770
Product Code BZD
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5905
Decision Date 2015-04-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LUNA CPAP AND AUTO-CPAP SYSTEM received FDA 510(k) clearance under submission number K141770, sponsored by 3B Medical, 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 2015-04-22.

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.