FDA 510(k)

NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses

N.º K: K173086 · 2017-11-07

SolicitanteVisioneering Technologies, Inc.

Fecha de decisión2017-11-07

Código de productoLPL

Comité asesorOP

DecisiónSubstantially Equivalent

Resumen del dispositivo

NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses is the device name listed in this FDA 510(k) record. The listed applicant is Visioneering Technologies, Inc.. It received FDA 510(k) clearance on 2017-11-07 under 510(k) number K173086. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses?

NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses is a medical device that received FDA 510(k) clearance on 2017-11-07. The listed applicant is Visioneering Technologies, Inc.. The 510(k) number is K173086.

When did NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses receive FDA 510(k) clearance?

NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses received FDA 510(k) clearance on 2017-11-07, under 510(k) number K173086.

Who is the listed applicant for NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses?

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

What is the FDA product code for NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses?

The FDA product code for NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses is LPL.

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: LPL)

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.