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FLASH PTA BALLON DILATATION CATHETER-5MM X 19MM X 135CM

K121175 Class II Traditional
Decision Date
2012-06-29
Sponsor / Applicant
Ostial Corporation

Technical Specification

510(k) Submission ID K121175
Product Code LIT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2012-06-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLASH PTA BALLON DILATATION CATHETER-5MM X 19MM X 135CM received FDA 510(k) clearance under submission number K121175, sponsored by Ostial Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-06-29.

Classification & Regulation

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