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CONTOUR EMBOLI PVA AND FASTRACKER-325 INFUSION CATHETER

K030966 Class II Traditional
Decision Date
2003-09-23
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K030966
Product Code NAJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3300
Decision Date 2003-09-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONTOUR EMBOLI PVA AND FASTRACKER-325 INFUSION CATHETER received FDA 510(k) clearance under submission number K030966, sponsored by 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 2003-09-23.

Classification & Regulation

This clearance is catalogued under FDA product code NAJ and 21 CFR 870.3300, within the Cardiovascular review panel as a Class II device.