Endoscopic Cytology Brushes

FDA 510(k) K791668 · Mill-Rose Laboratory

Substantially Equivalent

510(k) numberK791668

Submission

Device name
Endoscopic Cytology Brushes
Applicant
Mill-Rose Laboratory
Mchenry, IL, US
Received
August 28, 1979
Decision date
October 1, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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

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K250993Single Use Cytology Brush V (BC-V600P-3010)FDX · Traditional Olympus Medical Systems Corporation12/18/2025SE
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

More from United States Endoscopy Group, Inc.

510(k)DeviceDecision
K983124Mill-Rose Laboratories Transbronchial Needle Aspiration (Tbna) Cytology Procedural KitEOQ · Traditional 10/30/1998SE
K983122Mill-Rose Laboratories Transbronchial Needle Aspiration (Tbna) Combination…EOQ · Traditional 10/30/1998SE
K971275Mill-Rose Disposable Polypectomy SnareFDI · Traditional 05/23/1997SE
K962736Mill-Rose Laryngoscopic Injection NeedleEOQ · Traditional 07/29/1996SE
K960880Mill-Rose Blind Microbiology BrushEOQ · Traditional 04/29/1996SE
K954519Wang Transendoscopic Aspiration NeedleFBK · Traditional 12/22/1995SE
K951600Mill-Rose Rotatable Polypectomy SnareFDI · Traditional 12/18/1995SE
K954745Mill-Rose Rigid Scope Cleaning BrushesFEB · Traditional 11/27/1995SE
K951051Rite-Bite Biopsy ForcepsEOQ · Traditional 03/24/1995SE
K951048Rite-Bite Biopsy ForcepsFCL · Traditional 03/15/1995SE

Questions and answers

When was Endoscopic Cytology Brushes cleared by the FDA?

Endoscopic Cytology Brushes (K791668) received a 510(k) decision of Substantially Equivalent on October 1, 1979, 34 days after the submission was received.

What is the product code of K791668?

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