# Spaulding Clinical Research, LLC

- Location (FDA's records): West Bend, WI
- FDA decisions: 2 (2011–2015): 2 510(k) clearances
- Product codes: DPS (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 2 (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
- Mortara Instrument, Inc.: 1 (https://510kreport.com/company/mortara-instrument)
- Corscience GmbH & Co. KG: 1 (https://510kreport.com/company/corscience)

## Firms that cite its devices most
- Vales & Hills Biomedical Tech., Ltd.: 1 (https://510kreport.com/company/vales-hills-biomedical-tech)

## Its most-cited devices
- K150564: Spaulding Electrocardiograph 2100iQ (2015), cited by 1
- K110065: Spaulding IQ Electrocardiograph (2011), cited by 1

## Recent decisions
- K150564: Spaulding Electrocardiograph 2100iQ (Aug 12, 2015)
- K110065: Spaulding IQ Electrocardiograph (Mar 2, 2011)

Source page: https://510kreport.com/company/spaulding-clinical-research