meddevicedb.com FDA Device Reference

V-BAG WITH GBS COATING

K050195 Class II Traditional
Decision Date
2005-03-17
Sponsor / Applicant
Gish Biomedical, Inc.

Technical Specification

510(k) Submission ID K050195
Product Code DTN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4400
Decision Date 2005-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

V-BAG WITH GBS COATING received FDA 510(k) clearance under submission number K050195, 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 2005-03-17.

Classification & Regulation

This clearance is catalogued under FDA product code DTN and 21 CFR 870.4400, within the Cardiovascular review panel as a Class II device.