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ENDOBIONICS MICROSYRINGE (USYRINGE) INFUSION CATHETER

K040139 Class II Traditional
Decision Date
2004-02-18
Sponsor / Applicant
Endobionics, Inc.

Technical Specification

510(k) Submission ID K040139
Product Code KRA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1210
Decision Date 2004-02-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDOBIONICS MICROSYRINGE (USYRINGE) INFUSION CATHETER received FDA 510(k) clearance under submission number K040139, sponsored by Endobionics, 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 2004-02-18.

Classification & Regulation

This clearance is catalogued under FDA product code KRA and 21 CFR 870.1210, within the Cardiovascular review panel as a Class II device.