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Fountain ValveTip Infusion Catheter

K193082 Class II Traditional
Decision Date
2020-08-07
Sponsor / Applicant
Merit Medical Systems, Inc.

Technical Specification

510(k) Submission ID K193082
Product Code KRA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1210
Decision Date 2020-08-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Fountain ValveTip Infusion Catheter received FDA 510(k) clearance under submission number K193082, sponsored by Merit Medical Systems, 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 2020-08-07.

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.