meddevicedb.com FDA Device Reference

POLYSTAN HEART LUNG MACHINE SYS

K813034 Class II Traditional
Decision Date
1981-11-27
Sponsor / Applicant
Advocacy International, Ltd.

Technical Specification

510(k) Submission ID K813034
Product Code DTQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4220
Decision Date 1981-11-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POLYSTAN HEART LUNG MACHINE SYS received FDA 510(k) clearance under submission number K813034, 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 DTQ and 21 CFR 870.4220, within the Cardiovascular review panel as a Class II device.