# K932293: Cabot Medical Bipolar Cutting Forceps

- Pathway: 510(k) (Traditional)
- Applicant: Cabot Medical Corp.
- Decided: Jul 27, 1994 after 442 days
- Product code: KNS (Unit, Electrosurgical, Endoscopic (With Or Without Accessories))
- Device class: 2
- Regulation: 21 CFR 876.4300
- Recalls of this device: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
204 later devices descend from it; 2 cite it directly.
0 of 205 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K981916: Ligasure Vessel Sealing System (1998), 202 descendants of its own
- K051644: Valleylab Forcetriad Electrosurgical Generator (2005), 128 descendants of its own
- K031011: Ligasure 5MM Laparoscopic Sealer-Divider, Model LS1500 (2003), 114 descendants of its own
- K070162: Forcetriad Electrosurgical Generator; Ligasure Instruments (2007), 102 descendants of its own
- K092879: Ligasure 5MM Blunt Tip Laparoscopic Sealer-Divider (2009), 65 descendants of its own

## Recalls of this device
- Feb 19, 2007 · Not classified · Z-0615-2007: Product sterility may be compromised due to failure of the tray seal packaging
- Feb 19, 2007 · Not classified · Z-0613-2007: Product sterility may be compromised due to failure of the tray seal packaging
- Feb 19, 2007 · Not classified · Z-0614-2007: Product sterility may be compromised due to failure of the tray seal packaging

Source page: https://510kreport.com/device/K932293
Methodology: https://510kreport.com/methodology