# Hypertec, Inc.

- Location (FDA's records): Deer Field, IL
- FDA decisions: 2 (2000–2000): 2 510(k) clearances
- Product codes: CBF (2)
- Predicates its devices cite: 0 (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 that cite its devices most
- Pan-America Hyperbarics, Inc.: 1 (https://510kreport.com/company/pan-america-hyperbarics)
- Hyperbaric America, LLC: 1 (https://510kreport.com/company/hyperbaric-america)

## Its most-cited devices
- K002795: Model Hybrid 3200 Monoplace, Hyperbaric Therapy Systems (2000), cited by 2

## Recent decisions
- K002794: Model 5000 Multiplace Hyperbaric Therapy (Dec 6, 2000)
- K002795: Model Hybrid 3200 Monoplace, Hyperbaric Therapy Systems (Dec 6, 2000)

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