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CAMBRIDGE HEART MICRO-V ALTERNANS SENSOR, MODEL 20327-002

K002230 Class II Special
Decision Date
2000-08-18
Sponsor / Applicant
Cambridge Heart, Inc.

Technical Specification

510(k) Submission ID K002230
Product Code DRX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2360
Decision Date 2000-08-18
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CAMBRIDGE HEART MICRO-V ALTERNANS SENSOR, MODEL 20327-002 received FDA 510(k) clearance under submission number K002230, 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 2000-08-18.

Classification & Regulation

This clearance is catalogued under FDA product code DRX and 21 CFR 870.2360, within the Cardiovascular review panel as a Class II device.