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MODEL 5600B PROGRAMMER, PACEMAKER

K871986 Class III Traditional
Decision Date
1987-06-24
Sponsor / Applicant
Telectronics, Inc.

Technical Specification

510(k) Submission ID K871986
Product Code KRG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3700
Decision Date 1987-06-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 5600B PROGRAMMER, PACEMAKER received FDA 510(k) clearance under submission number K871986, sponsored by Telectronics, 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 1987-06-24.

Classification & Regulation

This clearance is catalogued under FDA product code KRG and 21 CFR 870.3700, within the Cardiovascular review panel as a Class III device.