# Apmtd, Inc.

- Location (FDA's records): Wilmington, MA
- FDA decisions: 2 (2023–2023): 2 510(k) clearances
- Product codes: DWA (2)
- Predicates its devices cite: 2 (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
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)

## Its most-cited devices
- K221491: Anivia SG1000 Pump Console (2023), cited by 1

## Recent decisions
- K230698: Anivia SG1000 Pump Console (Apr 18, 2023)
- K221491: Anivia SG1000 Pump Console (Feb 3, 2023)

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