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LARGE CENTRIFUGAL BLOOD PUMP, MODEL CP-2

K020529 Class II Traditional
Decision Date
2002-08-26
Sponsor / Applicant
A-Med Systems, Inc.

Technical Specification

510(k) Submission ID K020529
Product Code KFM
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4360
Decision Date 2002-08-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LARGE CENTRIFUGAL BLOOD PUMP, MODEL CP-2 received FDA 510(k) clearance under submission number K020529, sponsored by A-Med 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 2002-08-26.

Classification & Regulation

This clearance is catalogued under FDA product code KFM and 21 CFR 870.4360, within the Cardiovascular review panel as a Class II device.