meddevicedb.com FDA Device Reference

VICEROY INFLATION DEVICE

K040138 Class II Traditional
Decision Date
2004-02-13
Sponsor / Applicant
Merit Medical Systems, Inc.

Technical Specification

510(k) Submission ID K040138
Product Code MAV
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1650
Decision Date 2004-02-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VICEROY INFLATION DEVICE received FDA 510(k) clearance under submission number K040138, 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 2004-02-13.

Classification & Regulation

This clearance is catalogued under FDA product code MAV and 21 CFR 870.1650, within the Cardiovascular review panel as a Class II device.