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IMPLANTABLE ENDOCARDIAL POROUS TIP ELEC.

K801792 Class III Traditional
Decision Date
1980-10-23
Sponsor / Applicant
Telectronics, Inc.

Technical Specification

510(k) Submission ID K801792
Product Code DTB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 1980-10-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMPLANTABLE ENDOCARDIAL POROUS TIP ELEC. received FDA 510(k) clearance under submission number K801792, 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 1980-10-23.

Classification & Regulation

This clearance is catalogued under FDA product code DTB and 21 CFR 870.3680, within the Cardiovascular review panel as a Class III device.