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SINGLE PASS BLOOD CARDIOPLEGIA SPBC SYSTEM COMPONENTS

K944219 Class II Traditional
Decision Date
1995-06-30
Sponsor / Applicant
Gish Biomedical, Inc.

Technical Specification

510(k) Submission ID K944219
Product Code DTR
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4240
Decision Date 1995-06-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SINGLE PASS BLOOD CARDIOPLEGIA SPBC SYSTEM COMPONENTS received FDA 510(k) clearance under submission number K944219, 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 1995-06-30.

Classification & Regulation

This clearance is catalogued under FDA product code DTR and 21 CFR 870.4240, within the Cardiovascular review panel as a Class II device.