Sheath, Cystourethroscope W/ Obturator

FDA 510(k) K760179 · V. Mueller O.V. Baxter Healthcare Corp.

Substantially Equivalent

510(k) numberK760179

Submission

Device name
Sheath, Cystourethroscope W/ Obturator
Applicant
V. Mueller O.V. Baxter Healthcare Corp.
Mchenry, IL, US
Received
July 6, 1976
Decision date
December 2, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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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
K803292Field Suction DissectorGDI · Traditional 01/29/1981SE
K792383Kelman DipstickHOE · Traditional 12/11/1979SE
K771197Norton EndotrachealBTR · Traditional 08/16/1977SE
K771302Pfister-Schwartz Stone RetrieverFGO · Traditional 08/02/1977SE
K770959Bougie, Filiform, JacksonKBI · Traditional 06/14/1977SE
K770280Cord, Electrosurgical-Sterile & Dispos.KNS · Traditional 04/15/1977SE
K760851Converse Altar RetractorKAL · Traditional 03/10/1977SE
K761242Teflon Coated Resectoscope SheathFJL · Traditional 12/16/1976SE
K760273LithotriteFGK · Traditional 12/06/1976SE
K760189Stopcock, WaterlineFAJ · Traditional 12/02/1976SE

Questions and answers

When was Sheath, Cystourethroscope W/ Obturator cleared by the FDA?

Sheath, Cystourethroscope W/ Obturator (K760179) received a 510(k) decision of Substantially Equivalent on December 2, 1976, 149 days after the submission was received.

What is the product code of K760179?

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