# Laerdal Mfg. Corp.

- Location (FDA's records): Portland, OR
- FDA decisions: 5 (1988–1990): 5 510(k) clearances
- Product codes: LDD (3), MKJ (2)
- Predicates its devices cite: 0 (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

## Recent decisions
- K902429: Modified Heartstart Defibrillation Electrode (Sep 27, 1990)
- K900169: Modified Heartstart 2000 Defibrillation Electrode (Jan 26, 1990)
- K885186: Heartstart 2000 Defibrillation Electrode (Feb 23, 1989)
- K883341: Heartstart 1000 (Sep 12, 1988)
- K883344: Heartstart 1000S (Sep 12, 1988)

Source page: https://510kreport.com/company/laerdal-mfg