# K950877: Reusable Monopolar Forceps

- Pathway: 510(k) (Traditional)
- Applicant: Boston Surgical Products, Inc.
- Decided: Mar 9, 1995 after 10 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- 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; 1 cites 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
- K130669: Single Use & Multi Use Bipolar Forceps / Single Use & Multi Use Monopolar Forceps (2013), 1 descendant of its own
- K210315: Single Use Hand Switch Monopolar Forceps with Smoke Evacuation, Single Use Hand Switch Bipolar Forceps with Smoke Evacuation, Single Use Hand Switch Monopolar Forceps, Single Use Hand Switch Bipolar Forceps (2022), 0 descendants of its own

Source page: https://510kreport.com/device/K950877
Methodology: https://510kreport.com/methodology