Aviso: Este sitio agrega datos públicos oficiales de la FDA, ClinicalTrials.gov, PubMed y SEC EDGAR solo como referencia general. No constituye asesoramiento médico, diagnóstico, recomendaciones de tratamiento ni asesoramiento de inversión.

FDA 510(k)

Ready to use Nelaton Catheter

N.º K: K251178 · 2026-01-02

SolicitanteJamjoom Fullcare Corporation
Fecha de decisión2026-01-02
Código de productoEZD
Comité asesorGU
DecisiónSubstantially Equivalent

Resumen del dispositivo

Ready to use Nelaton Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Jamjoom Fullcare Corporation. It received FDA 510(k) clearance on 2026-01-02 under 510(k) number K251178. The device is classified under product code EZD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Ready to use Nelaton Catheter?

Ready to use Nelaton Catheter is a medical device that received FDA 510(k) clearance on 2026-01-02. The listed applicant is Jamjoom Fullcare Corporation. The 510(k) number is K251178.

When did Ready to use Nelaton Catheter receive FDA 510(k) clearance?

Ready to use Nelaton Catheter received FDA 510(k) clearance on 2026-01-02, under 510(k) number K251178.

Who is the listed applicant for Ready to use Nelaton Catheter?

The FDA 510(k) record lists Jamjoom Fullcare Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ready to use Nelaton Catheter?

The FDA product code for Ready to use Nelaton Catheter is EZD.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Dispositivos relacionados (Código: EZD)

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.

K261418Liquick X-treme, Liquick X-treme PlusTeleflex MedicalK260737Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Female (CH06 - CH16); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Straight (CH06 - CH18); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Coude (CH10 - CH18).ConvatecK261658LoFric Origo Pro CoudéWellspect ABK262045Luja SoftColoplast A.S.K260394Hydrophilic coated intermittent nalaton catheter for single use-ready to use (NCR)Hangzhou Jimushi Meditech Co., Ltd.K253295Coude Sleeved IC; Coude Plus Sleeved ICHollister Incorporated

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.

↑