meddevicedb.com FDA Device Reference

WM. HARVEY OVERPRESSURE SAFETY VALVE

K820297 Class II Traditional
Decision Date
1982-03-12
Sponsor / Applicant
C.R. Bard, Inc.

Technical Specification

510(k) Submission ID K820297
Product Code DTL
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4290
Decision Date 1982-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WM. HARVEY OVERPRESSURE SAFETY VALVE received FDA 510(k) clearance under submission number K820297, 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 1982-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code DTL and 21 CFR 870.4290, within the Cardiovascular review panel as a Class II device.