FCN-15X, Fiber Choledochonephroscope

FDA 510(k) K951191 · Pentax Precision Instrument Corp.

Substantially Equivalent

510(k) numberK951191

Submission

Device name
FCN-15X, Fiber Choledochonephroscope
Applicant
Pentax Precision Instrument Corp.
Miramar, FL, US
Received
March 16, 1995
Decision date
May 30, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FBN – Choledochoscope And Accessories, Flexible/Rigid
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

to examine and perform procedures within the bile ducts. For reusable, flexible endoscopes in this product code, validated reprocessing instructions and reprocessing validation data must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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More from Zhuhai Pusen Medical Technology Co., Ltd.

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K041397EG-3830UTITX · Traditional 06/09/2004SE
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K041395EG-3630URITX · Traditional 06/09/2004SE
K031789EG-3830UT, Video Ultrasound GastroscopeODG · Traditional 08/08/2003SE
K023401EG-3830UT, Video Ultrasound GastroscopeODG · Traditional 02/11/2003SE
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Questions and answers

When was FCN-15X, Fiber Choledochonephroscope cleared by the FDA?

FCN-15X, Fiber Choledochonephroscope (K951191) received a 510(k) decision of Substantially Equivalent on May 30, 1995, 75 days after the submission was received.

What is the product code of K951191?

The FDA product code is FBN – Choledochoscope And Accessories, Flexible/Rigid, a Class II (moderate risk) device regulated under 21 CFR 876.1500.