# Sentra Medical Devices, LLC

- Location (FDA's records): Canton, MI
- FDA decisions: 1 (2006–2006): 1 510(k) clearance
- Product codes: DRS (1)
- Predicates its devices cite: 1 (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
- American Pharmaseal Div. Ahsc: 1 (https://510kreport.com/company/american-pharmaseal-div-ahsc)

## Recent decisions
- K062342: Truepulse Disposable Invasive Blood Pressure Monitoring Kit (Sep 25, 2006)

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