ClearanceBrief
510(k) K221683 ยท FAJ Cystoscope And Accessories, Flexible/Rigid

CYSTO-NEPHRO VIDEOSCOPE (OLYMPUS CYF-V2), CYSTO-NEPHRO VIDEOSCOPE (OLYMPUS CYF-V2R), CYSTO-NEPHRO VIDEOSCOPE (OLYMPUS CYF-VH) and CYSTO-NEPHRO VIDEOSCOPE (OLYMPUS CYF-VHR)

ApplicantOlympus Medical Systems Corporation, Hachioji-Shi, JP
DecisionSubstantially Equivalent, Jan 20, 2023
ReceivedJun 10, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221683

DateFirm and productCodeLinked 510(k)
Jan 9, 2024Shirakawa Olympus Co., Ltd.
Model No. CYF-VH, CYSTO-NEPHRO VIDEOSCOPE
Open, Classified
FAJNone listed
Jan 9, 2024Shirakawa Olympus Co., Ltd.
Model No. CYF-VHR, CYSTO-NEPHRO VIDEOSCOPE
Open, Classified
FAJNone listed
Jan 9, 2024Shirakawa Olympus Co., Ltd.
Model No. CYF-V2, VISERA Cysto-Nephro Videoscope
Open, Classified
FAJNone listed
Jan 9, 2024Shirakawa Olympus Co., Ltd.
Model No. CYF-V2R, VISERA Cysto-Nephro Videoscope
Open, Classified
FAJNone listed
Nov 17, 2023Aizu Olympus Co., Ltd.
Cystonephroscope-endoscopic diagnosis and treatment within the bladder, urethra, and kidney Model Numbers: CYF-5, CYF-VH, CYF-VHR.
Open, Classified
FAJNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.