# K192499: Cyber Blade

- Pathway: 510(k) (Traditional)
- Applicant: SIDAM S.r.l.
- Decided: Jul 31, 2020 after 324 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- 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: 5 generations back to K871250 (1987). 17 ancestors in all.
2 later devices descend from it; 2 cite it directly.
1 of 20 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133272: Versacut + Tissue Morcellator, Lumenis, Ltd. (2014) Summary page 4.
- K041610: Morce Scope Set 8970 with Power Control 2303 and Suction Pump 2207, Richard Wolf Medical Instruments Corp. (2004) Summary page 4.

## Most influential descendants
- K260884: UNIDRIVE Select System (2026), 0 descendants of its own
- K251923: Medical Shaver System (Morcellator) (YSB-IIIA) (2026), 0 descendants of its own

## Indications for use
Cyber BLADE is intended for use under endoscopic visualization for the morcellation and removal of dissected benign prostatic hyperplasia (BPH) tissue during endoscopic surgical procedures in urology.

Source page: https://510kreport.com/device/K192499
Methodology: https://510kreport.com/methodology