# K030028: CPC by Soring GMBH

- Pathway: 510(k) (Special)
- Applicant: Soring GmbH Medizintechnik
- Decided: Jan 17, 2003 after 14 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: 2 generations back to K954171 (1996). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K993265: Soring GMBH, Arco 3000, Arco 2000, Arco 1000, MBC 601, MBC 600, Soring GmbH Medizintechnik (1999) Summary page 1.

## Indications for use
The devices are intended to cut and or coagulate soft biological tissue with gas-enhanced coagulation during surgical procedures. Typical users of this system are trained medical professionals

Source page: https://510kreport.com/device/K030028
Methodology: https://510kreport.com/methodology