Pentax Cystofiberscope, Model FCY-15P

FDA 510(k) K914008 · Pentax Precision Instrument Corp.

Substantially Equivalent

510(k) numberK914008

Submission

Device name
Pentax Cystofiberscope, Model FCY-15P
Applicant
Pentax Precision Instrument Corp.
Orangeburg, NY, US
Received
September 9, 1991
Decision date
January 10, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
FAJ – Cystoscope 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 urinary tract. 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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K253892Strauss Surgical Cystoscopes & Hysteroscopes (STS-2040-302ASA HD-endoscope, 4 x 302 mm…FAJ · Traditional Strauss Surgical USA04/16/2026SE
K253905PrimeSight UltraView SystemFAJ · Traditional Cogentix Medical, Inc.04/07/2026SE
K260271Strauss Surgical cystoscope, hysteroscope and accessories InstrumentsFAJ · Traditional American Medical Endoscopy, Inc.03/27/2026SE
K253226UV5000W HandleFAJ · Special Uroviu Corporation10/23/2025SE
K251140Zenflow Spring ScopeFAJ · Traditional Zenflow, Inc.09/23/2025SE
K252598Flexible Cystoscope (CY50H-20EU, CY50H-20US, CY55H-24EU, CY55H-24US)FAJ · Special Shanghai AnQing Medical Instrument Co., Ltd.09/15/2025SE
K250797UV5000 HandleFAJ · Traditional Uroviu Corporation09/11/2025SE
K243653KARL STORZ HOPKINS Telescopes for UrologyFAJ · Traditional Karl Storz SE & CO. KG08/13/2025SE

More from Karl Storz SE & CO. KG

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K041397EG-3830UTITX · Traditional 06/09/2004SE
K041396FG-36UX Fiber Ultrasound GastroscopeITX · Traditional 06/09/2004SE
K041395EG-3630URITX · Traditional 06/09/2004SE
K031789EG-3830UT, Video Ultrasound GastroscopeODG · Traditional 08/08/2003SE
K023401EG-3830UT, Video Ultrasound GastroscopeODG · Traditional 02/11/2003SE
K023376EB-1830T3, Video BronchoscopeEOQ · Special 10/16/2002SE
K021276FG-36UX Fiber Ultrasound GastroscopeODG · Traditional 09/12/2002SE
K021278EG-3630UR, Ultrasound Video GastroscopeODG · Traditional 09/06/2002SE
K013640EG-3630UR, Ultrasund Video GastroscopeFDS · Traditional 02/04/2002SE
K010740FG-36UX, Fiber Ultrasound GastroscopeODG · Traditional 04/17/2001SE

Questions and answers

When was Pentax Cystofiberscope, Model FCY-15P cleared by the FDA?

Pentax Cystofiberscope, Model FCY-15P (K914008) received a 510(k) decision of Substantially Equivalent on January 10, 1992, 123 days after the submission was received.

What is the product code of K914008?

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