meddevicedb.com FDA Device Reference

STERILIZATION

K943657 Class III Traditional
Decision Date
1996-06-24
Sponsor / Applicant
Telectronics Pacing Systems, Inc.

Technical Specification

510(k) Submission ID K943657
Product Code DTB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 1996-06-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILIZATION received FDA 510(k) clearance under submission number K943657, sponsored by Telectronics Pacing Systems, 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 1996-06-24.

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.