# K032092: Olympus Xcyf-TP3 Cystofiberscope/Nephrofiberscope

- Pathway: 510(k) (Traditional)
- Applicant: Olympus Optical Co., Ltd.
- Decided: Jul 16, 2003 after 9 days
- Product code: FCL (Forceps, Biopsy, Non-Electric)
- Device class: 1
- Regulation: 21 CFR 876.1075
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K931154 (1993). 12 ancestors in all.
No later device cites it as a predicate yet.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K993041: Olympus Xcyf-1T3 Oes Cystofiberscope/Nephrofiberscope Accessories and Ancillary Equipment, The Olympus Optical Co. (2000) Summary page 5.
- K011869: Xenf-DP Rhino-Laryngofiberscope, Its Accessories and Ancillary Equipment, The Olympus Optical Co. (2001) Summary page 5.

## Indications for use
This instrument has been designed to be used with an Olympus Light Source, documentation equipment, display monitor, suction pump, Endo-Therapy accessories, and other ancillary equipment for endoscopic diagnosis and treatment within the bladder, urethra and kidney.

Source page: https://510kreport.com/device/K032092
Methodology: https://510kreport.com/methodology