# K960757: Karl Storz Ureter Resectoscope

- Pathway: 510(k) (Traditional)
- Applicant: KARL STORZ Endoscopy-America, Inc.
- Decided: May 1, 1996 after 68 days
- Product code: FJL (Resectoscope)
- 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
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K060232: Trokamed GMBH Electrosurgical Instruments & Accessories (2006), 1 descendant of its own
- K261179: AlphaTriPart - Monopolar MIC Instruments (2026), 0 descendants of its own

## Indications for use
The KSEA ureter resectoscope is designed to be used for diagnostic and therapeutic procedures in the transurethral resection of tissue in the ureters and renal pelvis.

Source page: https://510kreport.com/device/K960757
Methodology: https://510kreport.com/methodology