# K102663: Aed Resectoscope

- Pathway: 510(k) (Traditional)
- Applicant: National Advanced Endoscopy Devices, Inc.
- Decided: Dec 30, 2010 after 106 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
Longest line of descent: 2 generations back to K895857 (1990). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K980302: Working Elements, Resectoscope Sheaths, Electrodes, Obturators, Endoscopes, Richard Wolf Medical Instruments Corp. (1998) Summary page 1.
- K954050: Resectoscopes, KARL STORZ Endoscopy-America, Inc. (1995) Summary page 1.

## Indications for use
Resectoscopes are used for endoscopically controlled ablation of tissue. They are used for examination, diagnosis and/or therapy in conjunction with endoscopic accessories in the various medical disciplines such as Urology and Gynecology.

Source page: https://510kreport.com/device/K102663
Methodology: https://510kreport.com/methodology