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WILLIAM HARVEY H-1500 BLOOD OXYGENATOR

K792039 Class II Traditional
Decision Date
1979-10-30
Sponsor / Applicant
C.R. Bard, Inc.

Technical Specification

510(k) Submission ID K792039
Product Code DTZ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4350
Decision Date 1979-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WILLIAM HARVEY H-1500 BLOOD OXYGENATOR received FDA 510(k) clearance under submission number K792039, 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 1979-10-30.

Classification & Regulation

This clearance is catalogued under FDA product code DTZ and 21 CFR 870.4350, within the Cardiovascular review panel as a Class II device.