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CCS IMPLANTABLE MAESTRO SERIES 100-HEART PACEMAKER

K850384 Class III Traditional
Decision Date
1985-03-21
Sponsor / Applicant
Cardiac Control Systems, Inc.

Technical Specification

510(k) Submission ID K850384
Product Code DXY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3610
Decision Date 1985-03-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CCS IMPLANTABLE MAESTRO SERIES 100-HEART PACEMAKER received FDA 510(k) clearance under submission number K850384, sponsored by Cardiac Control Systems, 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 1985-03-21.

Classification & Regulation

This clearance is catalogued under FDA product code DXY and 21 CFR 870.3610, within the Cardiovascular review panel as a Class III device.