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HOME HEALTH MONITORING SYSTEM

K010029 Class II Traditional
Decision Date
2001-06-29
Sponsor / Applicant
Avid Care Corp.

Technical Specification

510(k) Submission ID K010029
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2001-06-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOME HEALTH MONITORING SYSTEM received FDA 510(k) clearance under submission number K010029, sponsored by Avid Care Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2001-06-29.

Classification & Regulation

This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.