Single Use Cytology Brush V (BC-V600P-3010)

FDA 510(k) K250993 · Olympus Medical Systems Corporation

Substantially Equivalent

510(k) numberK250993

Submission

Device name
Single Use Cytology Brush V (BC-V600P-3010)
Applicant
Olympus Medical Systems Corporation
Hachioji-Shi, JP
Received
March 31, 2025
Decision date
December 18, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FDX – Endoscopic Cytology Brush
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

To collect cells for cytological evaluation.

Other 510(k)s with product code FDX

510(k)DeviceApplicantDecision
K220063Single Use Cytology BrushFDX · Traditional Zhejiang Chuangxiang Medical Technology Co., Ltd.07/28/2022SE
K192908Fusion Cytology Brush, CytoMax II Double Lumen Cytology BrushesFDX · Special Wilson-Cook Medical, Inc.11/14/2019SE
K191485Deflectable Brush Biopsy SetFDX · Traditional Cook Incorporated06/26/2019SE
K182231Brush Biopsy Set ; Deflectable Brush Biopsy SetFDX · Traditional Cook Incorporated05/01/2019SE
K181317Fusion Cytology Brush, CytoMax II Double Lumen Cytology BrushFDX · Traditional Wilson-Cook Medical, Inc.02/08/2019SE
K172663Cytology BrushFDX · Traditional Micro-Tech (Nanjing) Co., Ltd.03/05/2018SE
K171573Fusion Cytology Brush, CytoMax II Double Lumen Cytology BrushFDX · Traditional Wilson-Cook Medical, Inc.12/29/2017SE
K171607Bronchi and Gastrointestinal Cytology BrushFDX · Traditional Wilson-Cook Medical Inc./Cook Endoscopy07/31/2017SE
K151889Infinity ERCP Sampling DeviceFDX · Special United States Endoscopy Group, Inc.07/30/2015SE
K103437US Endoscopy Cytology BrushFDX · Special United States Endoscopy Group, Inc.12/23/2010SE

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Questions and answers

When was Single Use Cytology Brush V (BC-V600P-3010) cleared by the FDA?

Single Use Cytology Brush V (BC-V600P-3010) (K250993) received a 510(k) decision of Substantially Equivalent on December 18, 2025, 262 days after the submission was received.

What is the product code of K250993?

The FDA product code is FDX – Endoscopic Cytology Brush, a Class II (moderate risk) device regulated under 21 CFR 876.1500.