# Laerdal Medical A/S

- Location (FDA's records): Stavanger, NO
- FDA decisions: 4 (1999–2015): 4 510(k) clearances
- Product codes: LIX (1), BTA (1), CBP (1), BTM (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 2 (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
- Laerdal Medical Corp.: 2 (https://510kreport.com/company/laerdal-medical)
- Philips Medical Systems, Inc.: 1 (https://510kreport.com/company/philips-medical-systems)
- Bio-Detek, Inc.: 1 (https://510kreport.com/company/bio-detek)
- The Devilbiss Co.: 1 (https://510kreport.com/company/devilbiss)
- Ambu A/S: 1 (https://510kreport.com/company/ambu-a-s)

## Firms that cite its devices most
- Philips Medical Systems, Inc.: 1 (https://510kreport.com/company/philips-medical-systems)
- Laerdal Medical Corp.: 1 (https://510kreport.com/company/laerdal-medical)

## Its most-cited devices
- K122050: Cprmeter CPR Feedback Device (2012), cited by 2

## Recent decisions
- K132172: Neonatalie Resuscitator (Jan 15, 2015)
- K122050: Cprmeter CPR Feedback Device (Oct 22, 2012)
- K023805: Laerdal Paediatric Pocket Mask, Model 820050 (Feb 11, 2003)
- K993668: Laerdal Suction Unit,(4000) Model 78 00 20 (Dec 20, 1999)

Source page: https://510kreport.com/company/laerdal-medical-a-s