meddevicedb.com FDA Device Reference

LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICE

K902518 Class II Traditional
Decision Date
1990-10-16
Sponsor / Applicant
Pall Biomedical Products Co.

Technical Specification

510(k) Submission ID K902518
Product Code DTM
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4260
Decision Date 1990-10-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICE received FDA 510(k) clearance under submission number K902518, sponsored by Pall Biomedical Products Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1990-10-16.

Classification & Regulation

This clearance is catalogued under FDA product code DTM and 21 CFR 870.4260, within the Cardiovascular review panel as a Class II device.