SLIM Microcatheter

FDA 510(k) K260199 · Balt USA, LLC

Substantially Equivalent

510(k) numberK260199

Submission

Device name
SLIM Microcatheter
Applicant
Balt USA, LLC
Irvine, CA, US
Received
January 22, 2026
Decision date
July 13, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
QJP – Catheter, Percutaneous, Neurovasculature
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1250
Specialty
Cardiovascular

To provide vascular access to the neurovasculature for interventional or diagnostic procedures

Other 510(k)s with product code QJP

510(k)DeviceApplicantDecision
K26227770 NeuGlide CatheterQJP · Special Piraeus Medical, Inc.09/04/2026SE
K261176Zoom 4S CatheterQJP · Traditional Imperative Care, Inc.08/28/2026SE
K254071p17 XR MicrocatheterQJP · Traditional Wallaby Medical08/18/2026SE
K253901Millipede88 Access CatheterQJP · Traditional Perfuze, Ltd.07/09/2026SE
K261889Trevo Trak 21 MicrocatheterQJP · Special Stryker Neurovascular07/01/2026SE
K261808ISAAC Neurovascular Navigation CatheterQJP · Special Microvention Inc. d/b/a Terumo Neuro06/30/2026SE
K261549BOBBY Balloon Guide CatheterQJP · Special MicroVention, Inc., d/b/a Terumo Neuro06/09/2026SE
K253359Zenith Distal Access Long SheathQJP · Traditional Suzhou Zenith Vascular SciTech Limited05/22/2026SE
K254178SAYA 86 Radial Access Guide CatheterQJP · Traditional Asahi Intecc Co., Ltd.05/11/2026SE
K254046BosCATH Support CatheterQJP · Traditional Sonorous NV, Inc.04/21/2026SE

More from Sonorous NV, Inc.

510(k)DeviceDecision
K254223Next Generation 088 CatheterQJP · Traditional 04/16/2026SE
K254221Optima Coil System (OptiOne Coil System)HCG · Special 01/27/2026SE
K252569Carrier XL Delivery CatheterQJP · Special 10/22/2025SE
K252700Optima Coil System (Optima Packing Coil System)HCG · Special 09/26/2025SE
K243948Raptor Aspiration Catheter; Balt Aspiration Tubing SetNRY · Traditional 06/03/2025SE
K251383Prestige Coil System (Prestige Packing Line Extension)KRD · Special 05/30/2025SE
K242376Next Generation Access PlatformQJP · Traditional 12/30/2024SE
K242582Optima Coil System (OptiBlock Line Extension)HCG · Special 09/27/2024SE
K234083Next Generation Aspiration Catheter; Balt Aspiration Tubing SetNRY · Traditional 07/02/2024SE
K234074Next Generation Access CatheterQJP · Traditional 07/02/2024SE

Questions and answers

When was SLIM Microcatheter cleared by the FDA?

SLIM Microcatheter (K260199) received a 510(k) decision of Substantially Equivalent on July 13, 2026, 172 days after the submission was received.

What is the product code of K260199?

The FDA product code is QJP – Catheter, Percutaneous, Neurovasculature, a Class II (moderate risk) device regulated under 21 CFR 870.1250.