meddevicedb.com FDA Device Reference

BASIXTOUCH

K130566 Class II Special
Decision Date
2013-06-19
Sponsor / Applicant
Merit Medical Systems, Inc.

Technical Specification

510(k) Submission ID K130566
Product Code MAV
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1650
Decision Date 2013-06-19
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BASIXTOUCH received FDA 510(k) clearance under submission number K130566, sponsored by Merit Medical Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2013-06-19.

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.