# K093511: Soring MBC200/BCC140

- Pathway: 510(k) (Traditional)
- Applicant: Soring GmbH Medizintechnik
- Decided: Apr 16, 2010 after 154 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: 3 generations back to K954171 (1996). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K024059: MBC Series, Soring GmbH Medizintechnik (2003) Summary page 1.

## Indications for use
The Soring MBG200/BCC14o devices are intended to cut and or coagulate (soft) biological tissue during surgical procedures. Typical users of this system are trained medical professionals.

Source page: https://510kreport.com/device/K093511
Methodology: https://510kreport.com/methodology