# K960872: Cystoscope 0/15/30/70 Degrees

- Pathway: 510(k) (Traditional)
- Applicant: Pollux Endoscopy, Inc.
- Decided: May 7, 1996 after 64 days
- Product code: FAJ (Cystoscope And Accessories, Flexible/Rigid)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K925226 (1993). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K925226: Sight-Plus Arthroscope, American Medical Concepts, Inc. (1993) Summary page 1.

## Indications for use
This device is intended to provide access, illumination and allow observation or manipulation of body cavities, hollow organs, and canals.

Source page: https://510kreport.com/device/K960872
Methodology: https://510kreport.com/methodology