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CENTURION 2000 CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEM

K002604 Class II Traditional
Decision Date
2002-02-07
Sponsor / Applicant
Invivo Research, Inc.

Technical Specification

510(k) Submission ID K002604
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 2002-02-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CENTURION 2000 CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEM received FDA 510(k) clearance under submission number K002604, sponsored by Invivo Research, 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 2002-02-07.

Classification & Regulation

This clearance is catalogued under FDA product code DSI and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.