meddevicedb.com FDA Device Reference

POLYSTAN VERTICLUDE BLOOD PUMP

K813035 Class II Traditional
Decision Date
1981-11-27
Sponsor / Applicant
Advocacy International, Ltd.

Technical Specification

510(k) Submission ID K813035
Product Code DWB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4370
Decision Date 1981-11-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POLYSTAN VERTICLUDE BLOOD PUMP received FDA 510(k) clearance under submission number K813035, sponsored by Advocacy International, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1981-11-27.

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.