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HEALTHANYWHERE SYSTEM

K091220 Class II Traditional
Decision Date
2009-09-21
Sponsor / Applicant
Healthanywhere, an Igeacare System Company

Technical Specification

510(k) Submission ID K091220
Product Code DRG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2910
Decision Date 2009-09-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEALTHANYWHERE SYSTEM received FDA 510(k) clearance under submission number K091220, sponsored by Healthanywhere, an Igeacare System Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2009-09-21.

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.