meddevicedb.com FDA Device Reference

BMLS16-1

K172971 Class II Traditional
Decision Date
2018-07-08
Sponsor / Applicant
Biomedical Life Systems, Inc.

Technical Specification

510(k) Submission ID K172971
Product Code NUH
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5890
Decision Date 2018-07-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BMLS16-1 received FDA 510(k) clearance under submission number K172971, sponsored by Biomedical Life Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2018-07-08.

Classification & Regulation

This clearance is catalogued under FDA product code NUH and 21 CFR 882.5890, within the Neurology review panel as a Class II device.