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ALGO 3 NEWBORN HEARING SCREENER

K013137 Class II Special
Decision Date
2001-10-16
Sponsor / Applicant
Natus Medical, Inc.

Technical Specification

510(k) Submission ID K013137
Product Code GWJ
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1900
Decision Date 2001-10-16
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALGO 3 NEWBORN HEARING SCREENER received FDA 510(k) clearance under submission number K013137, sponsored by Natus Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2001-10-16.

Classification & Regulation

This clearance is catalogued under FDA product code GWJ and 21 CFR 882.1900, within the Neurology review panel as a Class II device.