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)

FA100 SCCD (Sequential Continuous Contraction Device)

N.º K: K162987 · 2017-02-14

SolicitanteFlowaid Medical Technologies, Corp
Fecha de decisión2017-02-14
Código de productoIPF
Comité asesorPM
DecisiónSubstantially Equivalent

Resumen del dispositivo

FA100 SCCD (Sequential Continuous Contraction Device) is the device name listed in this FDA 510(k) record. The listed applicant is Flowaid Medical Technologies, Corp. It received FDA 510(k) clearance on 2017-02-14 under 510(k) number K162987. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the FA100 SCCD (Sequential Continuous Contraction Device)?

FA100 SCCD (Sequential Continuous Contraction Device) is a medical device that received FDA 510(k) clearance on 2017-02-14. The listed applicant is Flowaid Medical Technologies, Corp. The 510(k) number is K162987.

When did FA100 SCCD (Sequential Continuous Contraction Device) receive FDA 510(k) clearance?

FA100 SCCD (Sequential Continuous Contraction Device) received FDA 510(k) clearance on 2017-02-14, under 510(k) number K162987.

Who is the listed applicant for FA100 SCCD (Sequential Continuous Contraction Device)?

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

What is the FDA product code for FA100 SCCD (Sequential Continuous Contraction Device)?

The FDA product code for FA100 SCCD (Sequential Continuous Contraction Device) is IPF.

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: IPF)

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.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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.

↑