FDA 510(k)

SureAx-Guide™

N.º K: K250203 · 2025-10-17

Fecha de decisión2025-10-17

Código de productoDQX

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

SureAx-Guide™ is the device name listed in this FDA 510(k) record. The listed applicant is Sureax Medical, LLC. It received FDA 510(k) clearance on 2025-10-17 under 510(k) number K250203. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the SureAx-Guide™?

SureAx-Guide™ is a medical device that received FDA 510(k) clearance on 2025-10-17. The listed applicant is Sureax Medical, LLC. The 510(k) number is K250203.

When did SureAx-Guide™ receive FDA 510(k) clearance?

SureAx-Guide™ received FDA 510(k) clearance on 2025-10-17, under 510(k) number K250203.

Who is the listed applicant for SureAx-Guide™?

The FDA 510(k) record lists Sureax Medical, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SureAx-Guide™?

The FDA product code for SureAx-Guide™ is DQX.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Dispositivos relacionados (Código: DQX)

K253146Hyperdrive 35 GuidewireRapid-Medical , Ltd.K261281CROSSLEAD Standard 035 and CROSSLEAD Stiff 035Filmecc Co., Ltd.K253667Accoat Guide WireSp Medical A/S K261640Merit MAK Nitinol/Gold-Tungsten Guide WireMerit Medical Ireland , Ltd.K254137InQwire Amplatz Guide WireMerit Medical Ireland, Ltd.K260544FMD Peripheral Guide Wire F-14 Flex 6; FMD Peripheral Guide Wire F-14 Tapered 40; FMD Peripheral Guide Wire F-18 Flex SP; FMD Peripheral Guide Wire F-18 DP 25; FMD Peripheral Guide Wire F-18 Tapered 40FMD Co., Ltd.

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.