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CONSTANT CARE LILAH HOME HEALTH MONITORING SYSTEM

K120941 Class II Traditional
Decision Date
2012-07-03
Sponsor / Applicant
Constant Care, LLC

Technical Specification

510(k) Submission ID K120941
Product Code DRG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2910
Decision Date 2012-07-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONSTANT CARE LILAH HOME HEALTH MONITORING SYSTEM received FDA 510(k) clearance under submission number K120941, sponsored by Constant Care, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-07-03.

Classification & Regulation

This clearance is catalogued under FDA product code DRG and 21 CFR 870.2910, within the Cardiovascular review panel as a Class II device.