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MEDILOG EXCEL 2 - HOLTER MANAGEMENT SYSTEM

K002544 Class II Special
Decision Date
2000-09-13
Sponsor / Applicant
Oxford Instruments

Technical Specification

510(k) Submission ID K002544
Product Code DQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1425
Decision Date 2000-09-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDILOG EXCEL 2 - HOLTER MANAGEMENT SYSTEM received FDA 510(k) clearance under submission number K002544, sponsored by Oxford Instruments. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-09-13.

Classification & Regulation

This clearance is catalogued under FDA product code DQK and 21 CFR 870.1425, within the Cardiovascular review panel as a Class II device.