Single-Use Flexible Cystoscope

FDA 510(k) K221580 · Hunan Vathin Medical Instrument Co., Ltd.

Substantially Equivalent

510(k) numberK221580

Submission

Device name
Single-Use Flexible Cystoscope
Applicant
Hunan Vathin Medical Instrument Co., Ltd.
Xiangtan, CN
Received
June 1, 2022
Decision date
November 18, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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).

Other 510(k)s with product code FAJ

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K260649OES ELITE Cystoscope and Accessories; Obturator, 17 Fr. (WA2C17BO); Obturator, 19.8 Fr.…FAJ · Traditional Olympus Winter & Ibe GmbH05/21/2026SE
K253696CFlex Cystoscope - Standard Deflection (0570-0455); CFlex Cystoscope - Reverse…FAJ · Traditional Verathon Medical (Canada) Ulc05/11/2026SE
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

510(k)DeviceDecision
K250232Vathin® Video Bronchoscope SystemEOQ · Traditional 07/25/2025SE
K251599Single-use Ureteral Access SheathFED · Special 07/03/2025SE
K250785Single-use Flexible UreteroscopeFGB · Traditional 05/06/2025SE
K243117Digital Video ProcessorFGB · Traditional 01/29/2025SE
K242416Single-use Flexible Bronchoscope: BC-E1C10, BC-E1C11, BC-E1C12, BC-E1E10, BC-E1E11…EOQ · Traditional 01/16/2025SE
K242535Single-use Flexible Cystoscope (CY-E2E01, CY-E2E01R, CY-E2F01, CY-E2F01R, CY-E2G01…FAJ · Traditional 12/18/2024SE
K241612Video Bronchoscope System; Single-use Flexible Bronchoscope (BC-S1E00-L, BC-S1H00-L…EOQ · Traditional 10/29/2024SE
K240167Single-use Ureteral Access SheathFED · Traditional 10/08/2024SE
K241434Video Ureteroscope SystemFGB · Special 10/04/2024SE
K231135Video Ureteroscope SystemFGB · Traditional 01/17/2024SE

Questions and answers

When was Single-Use Flexible Cystoscope cleared by the FDA?

Single-Use Flexible Cystoscope (K221580) received a 510(k) decision of Substantially Equivalent on November 18, 2022, 170 days after the submission was received.

What is the product code of K221580?

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