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ADVANCE ENFORCER 35 FOCAL FORCE PTA BALLOON CATHETER

K141322 Class II Traditional
Decision Date
2015-03-27
Sponsor / Applicant
Cook Incorporated

Technical Specification

510(k) Submission ID K141322
Product Code PNO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2015-03-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVANCE ENFORCER 35 FOCAL FORCE PTA BALLOON CATHETER received FDA 510(k) clearance under submission number K141322, sponsored by Cook Incorporated. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2015-03-27.

Classification & Regulation

This clearance is catalogued under FDA product code PNO and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.