# K052702: Misonix Inc. FS-1000-RF Bipolar Forceps Accessory

- Pathway: 510(k) (Traditional)
- Applicant: Misonix, Inc.
- Decided: Nov 21, 2005 after 54 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
Longest line of descent: 4 generations back to K923332 (1992). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K942710: Disposable Bipolar Coagulating Forceps, Boston Surgical Products, Inc. (1994) Summary page 1.
- K913108: Teflon Coated Electrodes/Electrodes Handles, Olsen Electrosurgical, Inc. (1991) Summary page 1.
- K051429: Claris Non-Stick Bipolar Forceps, Guenter Bissinger Medizintechnik GmbH (2005) Summary page 1.

## Indications for use
The Misonix Inc. FS-1000-RF Bipolar Forceps Accessory is indicated for use in bipolar procedures to grasp, manipulate, coagulate and/or transect tissues in the following specialities: Neurosurgery Plastic and Reconstructive Surgery General Surgery

Source page: https://510kreport.com/device/K052702
Methodology: https://510kreport.com/methodology