# Medi-Stim A/S

- Location (FDA's records): Brooklyn Park, MN
- FDA decisions: 2 (1999–2004): 2 510(k) clearances
- Product codes: DPW (1), ITX (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 4 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Koven Technology, Inc.: 1 (https://510kreport.com/company/koven-technology)
- Koven and Assoc., Inc.: 1 (https://510kreport.com/company/koven-and-assoc)
- Transonic Systems, Inc.: 1 (https://510kreport.com/company/transonic-systems)

## Firms that cite its devices most
- Medi-Stim Asa: 1 (https://510kreport.com/company/medi-stim)
- Transonic Systems, Inc.: 1 (https://510kreport.com/company/transonic-systems)
- Neoprobe Corp.: 1 (https://510kreport.com/company/neoprobe)

## Its most-cited devices
- K040228: Medi-Stim Veriq System, Model VQ1001 - VQ4122 (2004), cited by 2
- K992305: Medi-Stim Butterfly Flowmeter, Model BF1000-BF2004 (1999), cited by 2

## Recent decisions
- K040228: Medi-Stim Veriq System, Model VQ1001 - VQ4122 (Apr 29, 2004)
- K992305: Medi-Stim Butterfly Flowmeter, Model BF1000-BF2004 (Sep 8, 1999)

Source page: https://510kreport.com/company/medi-stim-a-s