# K983236: Bipolar HF Cable

- Pathway: 510(k) (Traditional)
- Applicant: Richard Wolf Medical Instruments Corp.
- Decided: Dec 4, 1998 after 80 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: 1 generation back to K943776 (1994). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K943776: Coagulator Cutter, Endoscopic Bipolar and Accessories, Richard Wolf Medical Instruments Corp. (1994) Summary page 1.

## Indications for use
The Bipolar HF Cables are used to connect adequately equipped R.Wolf HF instruments to the corresponding HF devices.

Source page: https://510kreport.com/device/K983236
Methodology: https://510kreport.com/methodology