# Naltiac Medical, Inc.

- Location (FDA's records): Dallas, TX
- FDA decisions: 3 (1996–1996): 3 510(k) clearances
- Product codes: DWF (2), DTL (1)
- Predicates its devices cite: 3 (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
- Dlp, Inc.: 2 (https://510kreport.com/company/dlp)
- Research Medical, Inc.: 1 (https://510kreport.com/company/research-medical)

## Recent decisions
- K961717: Nmi Retrograde Cardioplegia Cannula-RCCS (Jul 18, 1996)
- K961180: Nmi Antegrad Cardioplegia Cannula (Jun 21, 1996)
- K961181: Nmi Vein Graft Perfusion Set (Jun 21, 1996)

Source page: https://510kreport.com/company/naltiac-medical