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BRAUN SELECTIVE ANGIOGRAPHIC CATHETER

K950882 Class II Traditional
Decision Date
1995-08-17
Sponsor / Applicant
B.Braun Medical, Inc.

Technical Specification

510(k) Submission ID K950882
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 1995-08-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BRAUN SELECTIVE ANGIOGRAPHIC CATHETER received FDA 510(k) clearance under submission number K950882, sponsored by B.Braun Medical, 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 1995-08-17.

Classification & Regulation

This clearance is catalogued under FDA product code DQO and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.