meddevicedb.com FDA Device Reference

HEMASHIELD VANTAGE (VASCULAR GRAFT

K961847 Class II Traditional
Decision Date
1997-01-22
Sponsor / Applicant
Meadox Medicals, Div. Boston Scientific Corp.

Technical Specification

510(k) Submission ID K961847
Product Code DSY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3450
Decision Date 1997-01-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMASHIELD VANTAGE (VASCULAR GRAFT received FDA 510(k) clearance under submission number K961847, sponsored by Meadox Medicals, Div. Boston Scientific Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1997-01-22.

Classification & Regulation

This clearance is catalogued under FDA product code DSY and 21 CFR 870.3450, within the Cardiovascular review panel as a Class II device.