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BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT

K052524 Class II Special
Decision Date
2005-11-22
Sponsor / Applicant
Medtronic Perfusion Systems

Technical Specification

510(k) Submission ID K052524
Product Code DWF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4210
Decision Date 2005-11-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT received FDA 510(k) clearance under submission number K052524, sponsored by Medtronic Perfusion Systems. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2005-11-22.

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.