meddevicedb.com FDA Device Reference

BIOIMPEDANCE CARDIAC ANALYZING MEASURING SYSTEM

K080941 Class II Traditional
Decision Date
2009-06-18
Sponsor / Applicant
N.I. Medical, Ltd.

Technical Specification

510(k) Submission ID K080941
Product Code DSB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2770
Decision Date 2009-06-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOIMPEDANCE CARDIAC ANALYZING MEASURING SYSTEM received FDA 510(k) clearance under submission number K080941, sponsored by N.I. Medical, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2009-06-18.

Classification & Regulation

This clearance is catalogued under FDA product code DSB and 21 CFR 870.2770, within the Cardiovascular review panel as a Class II device.