meddevicedb.com FDA Device Reference

BILI-THERAPY PAD TYPE

K111547 Class II Traditional
Decision Date
2012-04-12
Sponsor / Applicant
Atom Medical Corporation

Technical Specification

510(k) Submission ID K111547
Product Code LBI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5700
Decision Date 2012-04-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BILI-THERAPY PAD TYPE received FDA 510(k) clearance under submission number K111547, sponsored by Atom Medical Corporation. 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 2012-04-12.

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.