meddevicedb.com FDA Device Reference

PACE*AID 10 A -PAD 10A- PACEMAKER OUTPUT DISPLAY &

K850596 Class II Traditional
Decision Date
1985-03-06
Sponsor / Applicant
Cardiac Resucitator Corp.

Technical Specification

510(k) Submission ID K850596
Product Code DRO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5550
Decision Date 1985-03-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PACE*AID 10 A -PAD 10A- PACEMAKER OUTPUT DISPLAY & received FDA 510(k) clearance under submission number K850596, sponsored by Cardiac Resucitator Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1985-03-06.

Classification & Regulation

This clearance is catalogued under FDA product code DRO and 21 CFR 870.5550, within the Cardiovascular review panel as a Class II device.