# Atlantean

- Location (FDA's records): Bonita Springs, FL
- FDA decisions: 2 (2010–2011): 2 510(k) clearances
- Names in FDA's records: Atlantean (1); Atlantean Corporation (1)
- Product codes: DQA (1), CAF (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
- Contec Medical System Co., Ltd.: 1 (https://510kreport.com/company/contec-medical-system)
- Hudson Respiratory Care, Inc.: 1 (https://510kreport.com/company/hudson-respiratory-care)

## Recent decisions
- K102719: Atlantean Trigger Nebulizer (Jul 1, 2011)
- K101568: Model SB100II Finger Pulse Oximeter (Sep 20, 2010)

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