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)

MPowRx Snoring Solution (also known as Good Morning Snore Solution)

N.º K: K193239 · 2020-01-03

SolicitanteMpowrx Health and Wellness Products 2012, Inc.
Fecha de decisión2020-01-03
Código de productoLRK
Comité asesorDE
DecisiónSubstantially Equivalent

Resumen del dispositivo

MPowRx Snoring Solution (also known as Good Morning Snore Solution) is the device name listed in this FDA 510(k) record. The listed applicant is Mpowrx Health and Wellness Products 2012, Inc.. It received FDA 510(k) clearance on 2020-01-03 under 510(k) number K193239. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the MPowRx Snoring Solution (also known as Good Morning Snore Solution)?

MPowRx Snoring Solution (also known as Good Morning Snore Solution) is a medical device that received FDA 510(k) clearance on 2020-01-03. The listed applicant is Mpowrx Health and Wellness Products 2012, Inc.. The 510(k) number is K193239.

When did MPowRx Snoring Solution (also known as Good Morning Snore Solution) receive FDA 510(k) clearance?

MPowRx Snoring Solution (also known as Good Morning Snore Solution) received FDA 510(k) clearance on 2020-01-03, under 510(k) number K193239.

Who is the listed applicant for MPowRx Snoring Solution (also known as Good Morning Snore Solution)?

The FDA 510(k) record lists Mpowrx Health and Wellness Products 2012, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MPowRx Snoring Solution (also known as Good Morning Snore Solution)?

The FDA product code for MPowRx Snoring Solution (also known as Good Morning Snore Solution) is LRK.

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: LRK)

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.

K262104Anti Snoring Mouthpiece (L09-BB, L09-PP, L09-TB, L09-BT, L09-TP, L09-PT, L09-TT)Ram.Shaw Pte., Ltd.K261912SnØreNegatØrDnB Innovations, LLCK261366VirtusSomnomed, Inc.K261251Snorbliss® Anti-Snoring DeviceEndeavor Commerce, LLCK261134Dormiva Anti-Snoring Mouth GuardKoncept Innovators, Inc.K252942ShaeferHShaeferh, LLC

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.

↑