meddevicedb.com FDA Device Reference

Bio-Medicus Life Support Catheter and Introducer

K201100 Class II Traditional
Decision Date
2021-07-15
Sponsor / Applicant
Medtronic, Inc.

Technical Specification

510(k) Submission ID K201100
Product Code DWF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4210
Decision Date 2021-07-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Bio-Medicus Life Support Catheter and Introducer received FDA 510(k) clearance under submission number K201100, sponsored by Medtronic, 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 2021-07-15.

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.