# K103841: Belimed Steam Sterilizer MST-V

- Pathway: 510(k) (Abbreviated)
- Applicant: Sauter AG
- Decided: Mar 15, 2011 after 83 days
- Product code: FLE (Sterilizer, Steam)
- Device class: 2
- Regulation: 21 CFR 880.6880
- 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 K033538 (2004). 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)
- K033538: Belimed Steam Sterilizer Top 5000, Series 4 - 8, Sauter AG (2004) Summary page 1.

## Indications for use
The Belimed Steam Sterilizers MST-V, models 6-0-6, 6-0-9, and 6-0-12 are designed for sterilization of non-porous and porous heat and moisture-stable materials used in healthcare facilities. The Belimed Steam Sterilizer MST-V, models 6-0-6, 6-0-9, and 6-0-12 are all equipped with the same factory-programmed Sterilization cycles and cycle parameters (Table 1). The Belimed Steam Sterilizers MST-V, models 6-0-6, 6-0-9, and 6-0-12 are available as a single door (VS1) prevacuum/gravity or double door (V52) prevacuum/gravity version.

Source page: https://510kreport.com/device/K103841
Methodology: https://510kreport.com/methodology