meddevicedb.com FDA Device Reference

MBA

K993057 Class II Special
Decision Date
1999-10-05
Sponsor / Applicant
Merit Medical Systems, Inc.

Technical Specification

510(k) Submission ID K993057
Product Code DTL
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4290
Decision Date 1999-10-05
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MBA received FDA 510(k) clearance under submission number K993057, 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 1999-10-05.

Classification & Regulation

This clearance is catalogued under FDA product code DTL and 21 CFR 870.4290, within the Cardiovascular review panel as a Class II device.