# Remco Italia S.P.A.

- Location (FDA's records): South Pedrino Di Vignate, Mi., IT
- FDA decisions: 3 (1985–2003): 3 510(k) clearances
- Product codes: DPS (2), MWJ (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 3 (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
- Braemar, Inc.: 1 (https://510kreport.com/company/braemar)
- Hewlett-Packard Co.: 1 (https://510kreport.com/company/hewlett-packard)
- Brentwood Medical Technology Corp.: 1 (https://510kreport.com/company/brentwood-medical-technology)
- Telemed Div.: 1 (https://510kreport.com/company/telemed-div)

## Firms that cite its devices most
- Dyansys, Inc.: 3 (https://510kreport.com/company/dyansys)

## Its most-cited devices
- K032200: Elan Digital 12 Channel Electrocardiograph (2003), cited by 3

## Recent decisions
- K032200: Elan Digital 12 Channel Electrocardiograph (Oct 3, 2003)
- K032276: Click Holter (Aug 27, 2003)
- K852770: Carioline (Electrocardiograph) (Aug 1, 1985)

Source page: https://510kreport.com/company/remco-italia