meddevicedb.com FDA Device Reference

Micro Ace™ Advanced Micro Access System

K232609 Class II Special
Decision Date
2023-09-27
Sponsor / Applicant
Merit Medical Systems, Inc.

Technical Specification

510(k) Submission ID K232609
Product Code DRE
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1310
Decision Date 2023-09-27
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Micro Ace™ Advanced Micro Access System received FDA 510(k) clearance under submission number K232609, 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 2023-09-27.

Classification & Regulation

This clearance is catalogued under FDA product code DRE and 21 CFR 870.1310, within the Cardiovascular review panel as a Class II device.