meddevicedb.com FDA Device Reference

EXTRACORPOREAL MEMBRANE OXYGENATION CATHETER

K882771 Class II Traditional
Decision Date
1988-09-27
Sponsor / Applicant
Cook, Inc.

Technical Specification

510(k) Submission ID K882771
Product Code DWF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4210
Decision Date 1988-09-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXTRACORPOREAL MEMBRANE OXYGENATION CATHETER received FDA 510(k) clearance under submission number K882771, sponsored by Cook, 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 1988-09-27.

Classification & Regulation

This clearance is catalogued under FDA product code DWF and 21 CFR 870.4210, within the Cardiovascular review panel as a Class II device.