# K924106: Biopsy Forceps

- Pathway: 510(k) (Traditional)
- Applicant: United States Endoscopy Group, Inc.
- Decided: Nov 24, 1992 after 103 days
- Product code: KNW (Instrument, Biopsy)
- Device class: 2
- Regulation: 21 CFR 876.1075
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
14 later devices descend from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K070330: Third Eye Retroscope Auxiliary Endoscopy System (2007), 13 descendants of its own
- K100624: Invendo C20 Colonoscopy System (2012), 6 descendants of its own
- K121582: Invendo C25 Colonoscopy System (2012), 5 descendants of its own
- K083180: Third Eye Retroscope Auxiliary Endoscopy System (2009), 5 descendants of its own
- K091783: Third Eye Retroscope Auxiliary Endoscope System (2009), 4 descendants of its own

Source page: https://510kreport.com/device/K924106
Methodology: https://510kreport.com/methodology