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LG1 INTELLIGENT MEDICAL VIGILANCE SYSTEM

K052446 Class II Traditional
Decision Date
2006-02-02
Sponsor / Applicant
Hoana Medical, Inc.

Technical Specification

510(k) Submission ID K052446
Product Code DRT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2006-02-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LG1 INTELLIGENT MEDICAL VIGILANCE SYSTEM received FDA 510(k) clearance under submission number K052446, sponsored by Hoana Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-02-02.

Classification & Regulation

This clearance is catalogued under FDA product code DRT and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.