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)

Kneevoice Cartilage Evaluation System (750-3600-001)

N.º K: K252076 · 2026-02-06

SolicitanteKneevoice, Inc.
Fecha de decisión2026-02-06
Código de productoDQD
Comité asesorCV
DecisiónSubstantially Equivalent

Resumen del dispositivo

Kneevoice Cartilage Evaluation System (750-3600-001) is the device name listed in this FDA 510(k) record. The listed applicant is Kneevoice, Inc.. It received FDA 510(k) clearance on 2026-02-06 under 510(k) number K252076. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Kneevoice Cartilage Evaluation System (750-3600-001)?

Kneevoice Cartilage Evaluation System (750-3600-001) is a medical device that received FDA 510(k) clearance on 2026-02-06. The listed applicant is Kneevoice, Inc.. The 510(k) number is K252076.

When did Kneevoice Cartilage Evaluation System (750-3600-001) receive FDA 510(k) clearance?

Kneevoice Cartilage Evaluation System (750-3600-001) received FDA 510(k) clearance on 2026-02-06, under 510(k) number K252076.

Who is the listed applicant for Kneevoice Cartilage Evaluation System (750-3600-001)?

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

What is the FDA product code for Kneevoice Cartilage Evaluation System (750-3600-001)?

The FDA product code for Kneevoice Cartilage Evaluation System (750-3600-001) is DQD.

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: DQD)

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.

K261494Smart Wireless Stethoscope (STEMO310);Smart Wireless Stethoscope (STEMO710);Smart Wireless Stethoscope (STEMO720);Smart Wireless Stethoscope (STEMO730)Shanghai Hulu Devices Co., Ltd.K261694CORE 300 Digital StethoscopeEko Health, Inc.K252915AiSteth®Ai Health Highway India Pvt., Ltd.K252089Tyto Stethoscope (G3)Tyto Care , Ltd.K252284eMurmur Heart AICsd LabsK252595Stethophone ProSparrow Acoustics, 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.

↑