# Seebreath AB

- Location (FDA's records): Bjarred, SE
- FDA decisions: 1 (2012–2012): 1 510(k) clearance
- Product codes: CCK (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Mercury Medical: 2 (https://510kreport.com/company/mercury-medical)

## Recent decisions
- K112840: Capnodura Combi & Capnodura Pedi CO2 Detector (Jul 13, 2012)

Source page: https://510kreport.com/company/seebreath