# Netech Corporation

- Location (FDA's records): Farmingdale, NY
- FDA decisions: 2 (1996–2019): 2 510(k) clearances
- Names in FDA's records: Netech Corporation (1); Netech Corp. (1)
- Product codes: DRL (2)
- 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
- Bc Group International, Inc.: 1 (https://510kreport.com/company/bc-group-international)
- Dongwon Medical Co., Ltd.: 1 (https://510kreport.com/company/dongwon-medical)

## Recent decisions
- K190437: Delta 3300 (Aug 28, 2019)
- K961595: Defibrillator Analyzer, Delta 1000 (Oct 29, 1996)

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