FDA 510(k)

Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D

N.º K: K252050 · 2026-03-20

SolicitanteOlympus Medical Systems Corporation

Fecha de decisión2026-03-20

Código de productoEOB

Comité asesorEN

DecisiónSubstantially Equivalent

Resumen del dispositivo

Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corporation. It received FDA 510(k) clearance on 2026-03-20 under 510(k) number K252050. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D?

Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D is a medical device that received FDA 510(k) clearance on 2026-03-20. The listed applicant is Olympus Medical Systems Corporation. The 510(k) number is K252050.

When did Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D receive FDA 510(k) clearance?

Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D received FDA 510(k) clearance on 2026-03-20, under 510(k) number K252050.

Who is the listed applicant for Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D?

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

What is the FDA product code for Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D?

The FDA product code for Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D is EOB.

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 Olympus Medical Systems Corporation como solicitante

K260856Disposable Distal Attachment D-201-13404 K260401EVIS EUS ULTRASOUND BRONCHOFIBERVIDEOSCOPE OLYMPUS BF-UCP190F (BF-UCP190F)K260824Gastrointestinal Videoscope Olympus GIF-2T1500 K261183EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)K261260HD Camera Head OLYMPUS CH-S200-08-LB K250993Single Use Cytology Brush V (BC-V600P-3010)

Ver todos los 36 dispositivos →

Dispositivos relacionados (Código: EOB)

K254299CLEARVISION Irrigation Sheath 0° (7241AS); CLEARVISION Irrigation Sheath 30° (7241BS); CLEARVISION Irrigation Sheath 45° (7241FS)Karl Storz SE & CO. KG K261544Hydro Irrigation SystemStryker Instruments K254133ENTity USB Videoscope SystemOptim, LLC K253184Video Rhinolaryngoscope System (Disposable Video Rhinolaryngoscope SP11A Endoscopic Video Processor M110B)Zhuhai Wesee Meditech Co., Ltd.K241731Outlook Surgical Versa One System (8900139)Resnent, LLC K243639Portare System (FA-001)Grumpy Innovation, 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.