# K092761: Proplate, Models 9641C, 9641F, P9641C, P9641F, 9642C, 9642F and P9642C

- Pathway: 510(k) (Special)
- Applicant: Bio Protech, Inc.
- Decided: Nov 24, 2009 after 76 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The PROPLATE is a disposable, single-use, neutral electrode, which provides a return path for high frequency electrical current to the ESU device.

Source page: https://510kreport.com/device/K092761
Methodology: https://510kreport.com/methodology