meddevicedb.com FDA Device Reference

BAIM TM CORONARY SINUS FLOW THERMAL

K810360 Class II Traditional
Decision Date
1981-03-11
Sponsor / Applicant
Electro-Catheter Corp.

Technical Specification

510(k) Submission ID K810360
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 1981-03-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BAIM TM CORONARY SINUS FLOW THERMAL received FDA 510(k) clearance under submission number K810360, sponsored by Electro-Catheter Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1981-03-11.

Classification & Regulation

This clearance is catalogued under FDA product code DQO and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.