meddevicedb.com FDA Device Reference

FLUORO-TEX CARDIOVASCULAR PATCH

K994032 Class II Traditional
Decision Date
2000-07-07
Sponsor / Applicant
Bridger Biomed, Inc.

Technical Specification

510(k) Submission ID K994032
Product Code DXZ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3470
Decision Date 2000-07-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLUORO-TEX CARDIOVASCULAR PATCH received FDA 510(k) clearance under submission number K994032, sponsored by Bridger Biomed, 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 2000-07-07.

Classification & Regulation

This clearance is catalogued under FDA product code DXZ and 21 CFR 870.3470, within the Cardiovascular review panel as a Class II device.