meddevicedb.com FDA Device Reference

SOFT VENOUS RESERVOIR

K955046 Class II Traditional
Decision Date
1996-01-11
Sponsor / Applicant
Gish Biomedical, Inc.

Technical Specification

510(k) Submission ID K955046
Product Code DTN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4400
Decision Date 1996-01-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOFT VENOUS RESERVOIR received FDA 510(k) clearance under submission number K955046, 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 1996-01-11.

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.