meddevicedb.com FDA Device Reference

IMPLANTABLE ELECTRODE BIPOLAR ADAPT

K840025 Class II Traditional
Decision Date
1984-05-23
Sponsor / Applicant
Telectronics, Inc.

Technical Specification

510(k) Submission ID K840025
Product Code DTD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3620
Decision Date 1984-05-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMPLANTABLE ELECTRODE BIPOLAR ADAPT received FDA 510(k) clearance under submission number K840025, 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 1984-05-23.

Classification & Regulation

This clearance is catalogued under FDA product code DTD and 21 CFR 870.3620, within the Cardiovascular review panel as a Class II device.