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ENDO-LOK L-40 ENDOCARDIAL PACING ELECT.

K760714 Class III Traditional
Decision Date
1976-12-14
Sponsor / Applicant
Coratomic, Inc.

Technical Specification

510(k) Submission ID K760714
Product Code DTB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 1976-12-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDO-LOK L-40 ENDOCARDIAL PACING ELECT. received FDA 510(k) clearance under submission number K760714, sponsored by Coratomic, 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 1976-12-14.

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.