meddevicedb.com FDA Device Reference

APEXPRO TELEMETRY SYSTEMS

K080251 Class II Traditional
Decision Date
2008-06-20
Sponsor / Applicant
Ge Medical Systems Information Technologies

Technical Specification

510(k) Submission ID K080251
Product Code MHX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 2008-06-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

APEXPRO TELEMETRY SYSTEMS received FDA 510(k) clearance under submission number K080251, sponsored by Ge Medical Systems Information Technologies. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2008-06-20.

Classification & Regulation

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