# The Henry G. Dietz Co., Inc.

- Location (FDA's records): Long Island City, NY
- FDA decisions: 2 (1991–1994): 2 510(k) clearances
- Product codes: NFB (1), KPR (1)
- 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
- K942581: Bes - Breath Exposure Synchronizer (Dec 12, 1994)
- K903504: Hala'tus 1 Oxygenator (Jan 28, 1991)

Source page: https://510kreport.com/company/henry-g-dietz