Micro Ace Gold Advanced Micro Access System

FDA 510(k) K242229 · Merit Medical Systems, Inc.

Substantially Equivalent

510(k) numberK242229

Submission

Device name
Micro Ace Gold Advanced Micro Access System
Applicant
Merit Medical Systems, Inc.
South Jordan, UT, US
Received
July 30, 2024
Decision date
January 15, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DRE – Dilator, Vessel, For Percutaneous Catheterization
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1310
Specialty
Cardiovascular

Other 510(k)s with product code DRE

510(k)DeviceApplicantDecision
K261310FlexTract Deflectable-Rotational Dilator Sheath SetDRE · Traditional Merit Medical Systems, Inc.07/27/2026SE
K253616ProtekDilate Vascular Access KitDRE · Special Sorin Group Italia S.R.L.12/19/2025SE
K251325VersaCross Connect™ Transseptal DilatorDRE · Special Baylis Medical Company, Inc.05/29/2025SE
K241720VersaCross Connect™ Transseptal DilatorDRE · Special Baylis Medical Company, Inc.07/12/2024SE
K233647VersaCross Connect™ Transseptal DilatorDRE · Special Baylis Medical Company, Inc.12/14/2023SE
K232609Micro Ace™ Advanced Micro Access SystemDRE · Special Merit Medical Systems, Inc.09/27/2023SE
K223472TightRail Guardian Motorized Dilator Sheath, 9 French (575-009); TightRail Guardian…DRE · Special Spectranetics, Inc.12/15/2022SE
K212784TightRail Guardian Motorized Dilator SheathDRE · Traditional Spectranetics, Inc.08/24/2022SE
K211679Xtractor deviceDRE · Traditional Xcardia Innovation , Ltd.02/17/2022SE
K210734Endovascular Dilator and SetsDRE · Special Cook Incorporated04/06/2021SE

More from Cook Incorporated

510(k)DeviceDecision
K261310FlexTract Deflectable-Rotational Dilator Sheath SetDRE · Traditional 07/27/2026SE
K262086PreludeSYNC™ Radial Compression DeviceDXC · Special 07/22/2026SE
K254073StatSeal DiscFRO · Traditional 05/13/2026SE
K251802STAR RF Ablation SystemGXI · Traditional 02/13/2026SE
K252892SCOUT MD Surgical Guidance SystemNEU · Traditional 12/19/2025SE
K250853Merit SyringeFMF · Special 11/04/2025SE
K251265Resilience Fully Covered Esophageal Stent SystemESW · Traditional 07/23/2025SE
K250909Prelude Wave Hydrophilic Sheath IntroducerDYB · Special 04/25/2025SE
K242873Ventrax™ Delivery SystemDQY · Special 01/15/2025SE
K241521Prelude Small O.D. Introducer Guide WireDQX · Traditional 12/10/2024SE

Questions and answers

When was Micro Ace Gold Advanced Micro Access System cleared by the FDA?

Micro Ace Gold Advanced Micro Access System (K242229) received a 510(k) decision of Substantially Equivalent on January 15, 2025, 169 days after the submission was received.

What is the product code of K242229?

The FDA product code is DRE – Dilator, Vessel, For Percutaneous Catheterization, a Class II (moderate risk) device regulated under 21 CFR 870.1310.