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MEDILOG EXCEL ECG ANALYSIS SYSTEM

K885256 Class II Traditional
Decision Date
1989-05-31
Sponsor / Applicant
Oxford Medical, Inc.

Technical Specification

510(k) Submission ID K885256
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 1989-05-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDILOG EXCEL ECG ANALYSIS SYSTEM received FDA 510(k) clearance under submission number K885256, sponsored by Oxford 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 1989-05-31.

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.