meddevicedb.com FDA Device Reference

CORONARY PRESSURE PERFUSION PUMP

K771764 Class II Traditional
Decision Date
1977-09-30
Sponsor / Applicant
3M Health Care, Sarns

Technical Specification

510(k) Submission ID K771764
Product Code DXS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4310
Decision Date 1977-09-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CORONARY PRESSURE PERFUSION PUMP received FDA 510(k) clearance under submission number K771764, 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 1977-09-30.

Classification & Regulation

This clearance is catalogued under FDA product code DXS and 21 CFR 870.4310, within the Cardiovascular review panel as a Class II device.