FDA 510(k)

Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff

N.º K: K182433 · 2018-12-17

SolicitanteShenzhen Caremed Medical Technology Co., Ltd.

Fecha de decisión2018-12-17

Código de productoDXQ

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Caremed Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2018-12-17 under 510(k) number K182433. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff?

Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff is a medical device that received FDA 510(k) clearance on 2018-12-17. The listed applicant is Shenzhen Caremed Medical Technology Co., Ltd.. The 510(k) number is K182433.

When did Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff receive FDA 510(k) clearance?

Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff received FDA 510(k) clearance on 2018-12-17, under 510(k) number K182433.

Who is the listed applicant for Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff?

The FDA 510(k) record lists Shenzhen Caremed Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff?

The FDA product code for Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff is DXQ.

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 Shenzhen Caremed Medical Technology Co., Ltd. como solicitante

K191279Disposable SpO2 Sensor K182751Reusable Temperature Probe K182755Disposable Temperature Probe K153184Caremed Reusable & Disposable SPO2 Sensors K153188Caremed patient cable and leadwires

Dispositivos relacionados (Código: DXQ)

K254287Medline Reusable Blood Pressure CuffMedline Industries, LP K260747YP-710T Series NIBP Cuff;YP-840T Series Disposable CuffNihon Kohden Corporation K253089NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722)Shenzhen Best Electronics Co., Ltd.K253964Disposable Neonatal NIBP Cuff (U1681S-C51N)Unimed Medical Supplies, Inc.K251745Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)Baxter Healthcare Corporation K250765Mangueira de Monitor de Presión Arterial de brazo AViTAAvita Corporation

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.