meddevicedb.com FDA Device Reference

HEALTH BUDDY APPLIANCE

K050567 Class II Special
Decision Date
2005-04-05
Sponsor / Applicant
Health Hero Network, Inc.

Technical Specification

510(k) Submission ID K050567
Product Code DRG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2910
Decision Date 2005-04-05
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEALTH BUDDY APPLIANCE received FDA 510(k) clearance under submission number K050567, 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 2005-04-05.

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.