# General Meditech, Inc.

- Location (FDA's records): Shanghai, CN
- FDA decisions: 2 (2009–2010): 2 510(k) clearances
- Product codes: MHX (1), DQA (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
- Shenzhen Mindray Bio-Medical Electronics Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-mindray-bio-medical-electronics)
- Beijing Choice Electronic Technololgy Co., Ltd.: 1 (https://510kreport.com/company/beijing-choice-electronic-technololgy)

## Recent decisions
- K092970: General Patient Monitors, Models: G3C/ G3D/ G3F/ G3G/ G3H (Feb 2, 2010)
- K082789: G1B Pulse Oximeter (Jan 7, 2009)

Source page: https://510kreport.com/company/general-meditech