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MODIFICATION TO HEALTH BUDDY APPLIANCE

K070543 Class II Special
Decision Date
2007-03-28
Sponsor / Applicant
Health Hero Network, Inc.

Technical Specification

510(k) Submission ID K070543
Product Code DRG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2910
Decision Date 2007-03-28
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO HEALTH BUDDY APPLIANCE received FDA 510(k) clearance under submission number K070543, sponsored by Health Hero Network, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2007-03-28.

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.