FDA 510(k)

core nova Complete Operating Room Endoscopy

N.º K: K151282 · 2016-01-12

SolicitanteRichard Wolf Medical Instruments Corp.

Fecha de decisión2016-01-12

Código de productoODA

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

core nova Complete Operating Room Endoscopy is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 2016-01-12 under 510(k) number K151282. The device is classified under product code ODA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the core nova Complete Operating Room Endoscopy?

core nova Complete Operating Room Endoscopy is a medical device that received FDA 510(k) clearance on 2016-01-12. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K151282.

When did core nova Complete Operating Room Endoscopy receive FDA 510(k) clearance?

core nova Complete Operating Room Endoscopy received FDA 510(k) clearance on 2016-01-12, under 510(k) number K151282.

Who is the listed applicant for core nova Complete Operating Room Endoscopy?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for core nova Complete Operating Room Endoscopy?

The FDA product code for core nova Complete Operating Room Endoscopy is ODA.

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: ODA)

K232406KARL STORZ OR1™ SCB CONTROL (WU300)Karl Storz SE & CO. KG K221929Smith+Nephew INTELLIO TabletSmith+Nephew K203566Tablet ApplicationSmith & Nephew K192876INTELLIO Tablet ApplicationSmith & Nephew K153205IDSS ForceTriad Control ModuleBlack Diamond Video, 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.