meddevicedb.com FDA Device Reference

S80 IMPLANTABLE CARDIAC PACING LEAD

K854963 Class III Traditional
Decision Date
1986-06-24
Sponsor / Applicant
Sorin Biomedica, Fiat, USA, Inc.

Technical Specification

510(k) Submission ID K854963
Product Code DTB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 1986-06-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

S80 IMPLANTABLE CARDIAC PACING LEAD received FDA 510(k) clearance under submission number K854963, sponsored by Sorin Biomedica, Fiat, USA, 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 1986-06-24.

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.