meddevicedb.com FDA Device Reference

MODEL APS ALTERNANS PROCESSING SYSTEM

K001034 Class II Special
Decision Date
2000-06-09
Sponsor / Applicant
Cambridge Heart, Inc.

Technical Specification

510(k) Submission ID K001034
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 2000-06-09
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL APS ALTERNANS PROCESSING SYSTEM received FDA 510(k) clearance under submission number K001034, sponsored by Cambridge Heart, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-06-09.

Classification & Regulation

This clearance is catalogued under FDA product code DPS and 21 CFR 870.2340, within the Cardiovascular review panel as a Class II device.