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NEOBLUE BLANKET LED PHOTOTHERAPY SYSTEM

K103589 Class II Traditional
Decision Date
2011-05-13
Sponsor / Applicant
Natus Medical Incorporated

Technical Specification

510(k) Submission ID K103589
Product Code LBI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5700
Decision Date 2011-05-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEOBLUE BLANKET LED PHOTOTHERAPY SYSTEM received FDA 510(k) clearance under submission number K103589, sponsored by Natus Medical Incorporated. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2011-05-13.

Classification & Regulation

This clearance is catalogued under FDA product code LBI and 21 CFR 880.5700, within the General Hospital review panel as a Class II device.