Berger Prostate Culture Cytology Brush

FDA 510(k) K880095 · Van-Tec, Inc.

Substantially Equivalent

510(k) numberK880095

Submission

Device name
Berger Prostate Culture Cytology Brush
Applicant
Van-Tec, Inc.
Spencer, IN, US
Received
January 12, 1988
Decision date
March 2, 1988
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.

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More from United States Endoscopy Group, Inc.

510(k)DeviceDecision
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K880098Van-Tec Auto Biopsy NeedleKNW · Traditional 03/02/1988SE
K880096Van-Tec Aspiration Biopsy System W/Collection CupKNW · Traditional 03/02/1988SE
K880094Van-Tec Endopyelotomy KnifeEMF · Traditional 02/29/1988SE
K874112Van-Tec Double Occlusion Balloon CatheterKOD · Traditional 02/11/1988SE
K871779Helical Stone Basket (Disposable)FFL · Traditional 06/17/1987SE
K871777Van-Tec Reusable Helical Stone BasketFFL · Traditional 06/17/1987SE
K870696Van-Tec Segura Stone Basket W/Protective SheathFFL · Traditional 03/30/1987SE
K870679Van-Tec Modular Flexible CystourethroscopeFBO · Traditional 03/30/1987SE
K870557Van-Tec Pumping SystemKOD · Traditional 03/30/1987SE

Questions and answers

When was Berger Prostate Culture Cytology Brush cleared by the FDA?

Berger Prostate Culture Cytology Brush (K880095) received a 510(k) decision of Substantially Equivalent on March 2, 1988, 50 days after the submission was received.

What is the product code of K880095?

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