# Amco International Manufacturing & Design, Inc.

- Location (FDA's records): Elizabeth, CO
- FDA decisions: 5 (2007–2009): 5 510(k) clearances
- Product codes: MKJ (4), MHX (1)
- Predicates its devices cite: 13 (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
- Philips Medical Systems, Inc.: 4 (https://510kreport.com/company/philips-medical-systems)
- Unipower Corp.: 2 (https://510kreport.com/company/unipower)
- R & D Batteries, Inc.: 2 (https://510kreport.com/company/r-d-batteries)
- Cardiac Science Corporation: 2 (https://510kreport.com/company/cardiac-science)
- Access Battery, Inc.: 1 (https://510kreport.com/company/access-battery)
- Medtronic Emergency Response Systems, Inc.: 1 (https://510kreport.com/company/medtronic-emergency-response-systems)
- Heartstream, Inc.: 1 (https://510kreport.com/company/heartstream)

## Recent decisions
- K091548: Amco Replacement Battery for Philips Medical Models BT1 and M5070A (Aug 7, 2009)
- K082861: Amco Replacement Battery for Powerheart Aed, Non-Rechargeable, Model 2L561; G3, Non-Rechargable, Model 7L561 (Nov 25, 2008)
- K073716: Life+Cel or Lifecel Battery (Apr 11, 2008)
- K072596: Life+Cel or Lifecel Battery Pack, Model 5L500 (Jan 24, 2008)
- K071164: Life+Cel Battery (Dec 7, 2007)

Source page: https://510kreport.com/company/amco-international-manufacturing-design