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)

Contact Lens Case (multiple brand name)

N.º K: K160005 · 2016-06-07

SolicitanteDanyang Chanxin Glasses Cases Factory
Fecha de decisión2016-06-07
Código de productoLRX
Comité asesorOP
DecisiónSubstantially Equivalent

Resumen del dispositivo

Contact Lens Case (multiple brand name) is the device name listed in this FDA 510(k) record. The listed applicant is Danyang Chanxin Glasses Cases Factory. It received FDA 510(k) clearance on 2016-06-07 under 510(k) number K160005. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Contact Lens Case (multiple brand name)?

Contact Lens Case (multiple brand name) is a medical device that received FDA 510(k) clearance on 2016-06-07. The listed applicant is Danyang Chanxin Glasses Cases Factory. The 510(k) number is K160005.

When did Contact Lens Case (multiple brand name) receive FDA 510(k) clearance?

Contact Lens Case (multiple brand name) received FDA 510(k) clearance on 2016-06-07, under 510(k) number K160005.

Who is the listed applicant for Contact Lens Case (multiple brand name)?

The FDA 510(k) record lists Danyang Chanxin Glasses Cases Factory as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Contact Lens Case (multiple brand name)?

The FDA product code for Contact Lens Case (multiple brand name) is LRX.

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: LRX)

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.

K252175LANDR Contact LENS CaseFourth Axis, LLCK250495MINI VP1 (PL67_F); MINI VP1 (PL61_F)Avizor S.A.K240095CAREUS Contact Lens Case (Model 1, Model 2, Model 3, Model 4, Model 5, Model 6)Shanghai Care US Medical Product Co., Ltd.K231123Phoenix Contact Lens Case - dome top flat pack (CL-01); Phoenix Contact Lens Case - classic flat pack (CL-02); Phoenix Contact Lens Case - sunglass shape flat pack (CL-03)Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.K173538Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODiscAlcon Laboratories, Inc.K172925Contact Lens Case, Model: A-1, B-1P L Overseas Limited

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.

↑