FDA 510(k)

D Camera Controller

N.º K: K211332 · 2021-10-01

SolicitanteRichard Wolf Medical Instruments Corporation

Fecha de decisión2021-10-01

Código de productoFET

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

D Camera Controller is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corporation. It received FDA 510(k) clearance on 2021-10-01 under 510(k) number K211332. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the D Camera Controller?

D Camera Controller is a medical device that received FDA 510(k) clearance on 2021-10-01. The listed applicant is Richard Wolf Medical Instruments Corporation. The 510(k) number is K211332.

When did D Camera Controller receive FDA 510(k) clearance?

D Camera Controller received FDA 510(k) clearance on 2021-10-01, under 510(k) number K211332.

Who is the listed applicant for D Camera Controller?

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

What is the FDA product code for D Camera Controller?

The FDA product code for D Camera Controller is FET.

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

Otros registros que enlistan a Richard Wolf Medical Instruments Corporation como solicitante

K231291Perforated Baskets K230194HF Surgery Generator 400KHZ K212808Logic Hd camera head green, System green K203226TELESCOPE 0 O 10MM WL 305MM / TELESCOPE 30 O 10MM WL 305MM / TELESCOPE 50 O 10MM WL 305MM, TELESCOPE 0 O 10MM WL 440MM / TELESCOPE 30 O 10MM WL 440MM / TELESCOPE 50 O 10MM WL 440MM K201897Sensor-Ureterorenoscope 9 FR WL 600 MM (short RIWO D-URS), Adapter For Controller 5525 K200617Logic HD Camera Controller, Logic HD Lite Camera Controller, Logic 4K Camera Contoller, Adapter for Controller 5525

Ver todos los 11 dispositivos →

Dispositivos relacionados (Código: FET)

K2620794K Camera Head OLYMPUS CH-S700-08-LBOlympus Medical Systems Corp.K261880FUJIFILM Processor EP-8000;Balloon Controller PB-30;Endoscopy Support Program EW10-VM01Fujifilm Corporation K261260HD Camera Head OLYMPUS CH-S200-08-LBOlympus Medical Systems Corporation K251734ProVee Video Processing Unit (PV-003)Proverum Limited K250462UL UHD-Clear View 4K Camera System (UL-3Chip 4K)Univlabs Technologies Private Limited K250204Endoscopic Camera SystemShenzhen Sophway Technology Co., Ltd.

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.