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CARDIOTOMY RESERVOIR BRS-XXX & HOLDER BRS-HXX

K851004 Class II Traditional
Decision Date
1985-05-16
Sponsor / Applicant
Gish Biomedical, Inc.

Technical Specification

510(k) Submission ID K851004
Product Code DTP
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4230
Decision Date 1985-05-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CARDIOTOMY RESERVOIR BRS-XXX & HOLDER BRS-HXX received FDA 510(k) clearance under submission number K851004, sponsored by Gish Biomedical, 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 1985-05-16.

Classification & Regulation

This clearance is catalogued under FDA product code DTP and 21 CFR 870.4230, within the Cardiovascular review panel as a Class II device.