meddevicedb.com FDA Device Reference

WILLIAM HARVEY H-625 ARTERIAL FILTER

K820472 Class II Traditional
Decision Date
1982-03-15
Sponsor / Applicant
C.R. Bard, Inc.

Technical Specification

510(k) Submission ID K820472
Product Code DTM
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4260
Decision Date 1982-03-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WILLIAM HARVEY H-625 ARTERIAL FILTER received FDA 510(k) clearance under submission number K820472, sponsored by C.R. Bard, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1982-03-15.

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.