FDA 510(k)

SOTA Cloud Smart Sensor (1.5)

N.º K: K251793 · 2026-03-03

Fecha de decisión2026-03-03

Código de productoMUH

Comité asesorDE

DecisiónSubstantially Equivalent

Resumen del dispositivo

SOTA Cloud Smart Sensor (1.5) is the device name listed in this FDA 510(k) record. The listed applicant is Sota Cloud Corp.. It received FDA 510(k) clearance on 2026-03-03 under 510(k) number K251793. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the SOTA Cloud Smart Sensor (1.5)?

SOTA Cloud Smart Sensor (1.5) is a medical device that received FDA 510(k) clearance on 2026-03-03. The listed applicant is Sota Cloud Corp.. The 510(k) number is K251793.

When did SOTA Cloud Smart Sensor (1.5) receive FDA 510(k) clearance?

SOTA Cloud Smart Sensor (1.5) received FDA 510(k) clearance on 2026-03-03, under 510(k) number K251793.

Who is the listed applicant for SOTA Cloud Smart Sensor (1.5)?

The FDA 510(k) record lists Sota Cloud Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOTA Cloud Smart Sensor (1.5)?

The FDA product code for SOTA Cloud Smart Sensor (1.5) is MUH.

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: MUH)

K252570EzSensor HD, EzSensor UHDQpix Solutions, Inc.K250687Cocoon Solo (DX-7020s)Dexcowin Global, Inc.K251206Digital X-Ray DentiMax Pro Imaging SystemDentimax, Inc.K240040VistaPano S Ceph 2.0 (VistaPano S Ceph); VistaPano S 2.0 (VistaPano S); ProVecta S-Pan Ceph 2.0 (ProVecta S-Pan Ceph); ProVecta S-Pan 2.0 (ProVecta S-Pan)VATECH Co., Ltd.K242778X Sensor (Model: IOS-A15IF, HDI-15DGF)Qpix Solutions, Inc.K241649DUO1 and DUO2Zinnovi, Inc.

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.