meddevicedb.com FDA Device Reference

TandemHeart Pump and Escort Controller

K202751 Class II Traditional
Decision Date
2021-03-26
Sponsor / Applicant
Cardiacassist, Inc.

Technical Specification

510(k) Submission ID K202751
Product Code QNR
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4100
Decision Date 2021-03-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TandemHeart Pump and Escort Controller received FDA 510(k) clearance under submission number K202751, sponsored by Cardiacassist, 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 2021-03-26.

Classification & Regulation

This clearance is catalogued under FDA product code QNR and 21 CFR 870.4100, within the Cardiovascular review panel as a Class II device.