meddevicedb.com FDA Device Reference

BLOOD PUMP MODEL 7000

K780942 Class II Traditional
Decision Date
1978-06-19
Sponsor / Applicant
3M Health Care, Sarns

Technical Specification

510(k) Submission ID K780942
Product Code DWB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4370
Decision Date 1978-06-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BLOOD PUMP MODEL 7000 received FDA 510(k) clearance under submission number K780942, sponsored by 3M Health Care, Sarns. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1978-06-19.

Classification & Regulation

This clearance is catalogued under FDA product code DWB and 21 CFR 870.4370, within the Cardiovascular review panel as a Class II device.