# Mec Dynamics Corp

- Location (FDA's records): Santa Clara, CA
- FDA decisions: 4 (2009–2013): 4 510(k) clearances
- Product codes: LCP (3), GKR (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (1 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
- Provalis Diagnostics, Ltd.: 1 (https://510kreport.com/company/provalis-diagnostics)
- Hemocue, Inc.: 1 (https://510kreport.com/company/hemocue)

## Its most-cited devices
- K091400: Modification to Avie A1C Test System (2009), cited by 1

## Recent decisions
- K121752: Avie Total HB Test System (Jan 7, 2013)
- K093548: Avie A1C Test System (Jul 20, 2011)
- K091400: Modification to Avie A1C Test System (Jun 11, 2009)
- K081269: Avie A1C Test System (Mar 20, 2009)

Source page: https://510kreport.com/company/mec-dynamics