# Anrad Corp.

- Location (FDA's records): Peabody, MA
- FDA decisions: 2 (2004–2005): 2 510(k) clearances
- Product codes: MQB (2)
- Predicates its devices cite: 4 (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
- Sterling Diagnostic Imaging, Inc.: 2 (https://510kreport.com/company/sterling-diagnostic-imaging)
- Fujifilm Medical System U.S.A., Inc.: 1 (https://510kreport.com/company/fujifilm-medical-system-usa)

## Its most-cited devices
- K042821: Digital Detector, Model GR17 (2004), cited by 1

## Recent decisions
- K052136: GR17 Digital Detector (Aug 25, 2005)
- K042821: Digital Detector, Model GR17 (Oct 22, 2004)

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