FDA 510(k)

lntravascular Administration Sets with Stopcock and Manifold

N.º K: K223175 · 2023-03-10

SolicitanteBaxter Healthcare Corporation

Fecha de decisión2023-03-10

Código de productoFMG

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

lntravascular Administration Sets with Stopcock and Manifold is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corporation. It received FDA 510(k) clearance on 2023-03-10 under 510(k) number K223175. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the lntravascular Administration Sets with Stopcock and Manifold?

lntravascular Administration Sets with Stopcock and Manifold is a medical device that received FDA 510(k) clearance on 2023-03-10. The listed applicant is Baxter Healthcare Corporation. The 510(k) number is K223175.

When did lntravascular Administration Sets with Stopcock and Manifold receive FDA 510(k) clearance?

lntravascular Administration Sets with Stopcock and Manifold received FDA 510(k) clearance on 2023-03-10, under 510(k) number K223175.

Who is the listed applicant for lntravascular Administration Sets with Stopcock and Manifold?

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

What is the FDA product code for lntravascular Administration Sets with Stopcock and Manifold?

The FDA product code for lntravascular Administration Sets with Stopcock and Manifold is FMG.

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

Otros registros que enlistan a Baxter Healthcare Corporation como solicitante

K251745Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)K251640SIGMA Spectrum Infusion Pump with Master Drug Library K251636Spectrum IQ Infusion System with Dose IQ Safety Software (3570009)K243529Solution Administration Sets K242339Intravascular Extension Sets and Accessories K242390Novum IQ Syringe Pump (40800BAXUS)

Ver todos los 44 dispositivos →

Dispositivos relacionados (Código: FMG)

K242255Qitexio® 4-Way Stopcock (QIT014)Medex K223499Three Way Stop CockM/S Romsons International K211204SafePort(TM) Manifold (or Stopcock)Elcam Medical Acal K210516Clicky CrossYomura Technologies, Inc.K190539TurnSignal Stopcocks Sterile, TurnSignal Stopcocks Buld Non Sterile, TurnSignal Stopcocks with Manifolds Sterile, TurnSignal Stopcocks with Manifolds Bulk Non SterileMonumedical, LLC K190489Elcam Stopcocks and ManifoldsElcam Medical Acal

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.