# K955052: Olympus FD-1/2-1 Hot Biopsy Forceps

- Pathway: 510(k) (Traditional)
- Applicant: Olympus America, Inc.
- Decided: Jan 24, 1996 after 79 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.
16 later devices descend from it; 2 cite it directly.
0 of 17 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
- K062517: Electrosurgical Hemostatic Forceps Series (2006), 10 descendants of its own
- K101657: Radial 4 Hot Biopsy Forceps Box 5; Radial Jaw 4 Hot Biopsy Forceps Box 20; Radial Jaw 4 Hot Biopsy Forceps Box 40 (2010), 4 descendants of its own
- K151474: Fujifilm Diathermic Slitter (FlushKnife), Diathermic Slitter (ClutchCutter) (2016), 3 descendants of its own
- K161186: Fujifilm Diathermic Slitter (FlushKnife), Fujifilm Diathermic Slitter (ClutchCutter) (2016), 2 descendants of its own
- K212423: EndoDrill® Model X (2023), 1 descendant of its own

Source page: https://510kreport.com/device/K955052
Methodology: https://510kreport.com/methodology