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)

Klinly Ultrasonic Tongue Cleaner

N.º K: K181986 · 2019-09-06

SolicitanteKea Products, Ltd.
Fecha de decisión2019-09-06
Código de productoQIA
Comité asesorDE
DecisiónSubstantially Equivalent

Resumen del dispositivo

Klinly Ultrasonic Tongue Cleaner is the device name listed in this FDA 510(k) record. The listed applicant is Kea Products, Ltd.. It received FDA 510(k) clearance on 2019-09-06 under 510(k) number K181986. The device is classified under product code QIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Klinly Ultrasonic Tongue Cleaner?

Klinly Ultrasonic Tongue Cleaner is a medical device that received FDA 510(k) clearance on 2019-09-06. The listed applicant is Kea Products, Ltd.. The 510(k) number is K181986.

When did Klinly Ultrasonic Tongue Cleaner receive FDA 510(k) clearance?

Klinly Ultrasonic Tongue Cleaner received FDA 510(k) clearance on 2019-09-06, under 510(k) number K181986.

Who is the listed applicant for Klinly Ultrasonic Tongue Cleaner?

The FDA 510(k) record lists Kea Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Klinly Ultrasonic Tongue Cleaner?

The FDA product code for Klinly Ultrasonic Tongue Cleaner is QIA.

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

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.

↑