# K932266: Symbiosis Dispos Gastro Biopsy Forceps W/Reuse Han

- Pathway: 510(k) (Traditional)
- Applicant: Symbiosis Corp.
- Decided: Mar 15, 1994 after 329 days
- Product code: KGE (Forceps, Biopsy, Electric)
- Device class: 2
- Regulation: 21 CFR 876.4300
- 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; 2 cite 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. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K033593: Reprocessed Single Use Devices Biopsy Forceps (2003), 0 descendants of its own
- K022751: Reprocessed Used Disposable Hot and Cold Biopsy Forceps (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K932266
Methodology: https://510kreport.com/methodology