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TENDERFLOW PERIATRIC ARTERIAL CANNULA

K063618 Class II Special
Decision Date
2007-03-13
Sponsor / Applicant
Terumo Cardiovascular Systems Corp.

Technical Specification

510(k) Submission ID K063618
Product Code DWF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4210
Decision Date 2007-03-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TENDERFLOW PERIATRIC ARTERIAL CANNULA received FDA 510(k) clearance under submission number K063618, sponsored by Terumo Cardiovascular Systems Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2007-03-13.

Classification & Regulation

This clearance is catalogued under FDA product code DWF and 21 CFR 870.4210, within the Cardiovascular review panel as a Class II device.