meddevicedb.com FDA Device Reference

MX1002 CABLE-CAL TM

K880696 Class II Traditional
Decision Date
1988-06-15
Sponsor / Applicant
Medex, Inc.

Technical Specification

510(k) Submission ID K880696
Product Code DXG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1435
Decision Date 1988-06-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MX1002 CABLE-CAL TM received FDA 510(k) clearance under submission number K880696, sponsored by Medex, 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 1988-06-15.

Classification & Regulation

This clearance is catalogued under FDA product code DXG and 21 CFR 870.1435, within the Cardiovascular review panel as a Class II device.