# Rand S.R.L.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 4 (2006–2016): 4 510(k) clearances
- Product codes: DTQ (2), LGZ (2)
- Predicates its devices cite: 8 (2 its own); citations of its devices by later devices: 4 (2 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Cobe Cardiovascular, Inc.: 2 (https://510kreport.com/company/cobe-cardiovascular)
- Terumo Cardiovascular Systems Corp.: 2 (https://510kreport.com/company/terumo-cardiovascular-systems)
- Belmont Instrument Corp.: 1 (https://510kreport.com/company/belmont-instrument)
- Rocky Mountain Research, Inc.: 1 (https://510kreport.com/company/rocky-mountain-research)

## Firms that cite its devices most
- Lifebridge Medizintechnik AG: 1 (https://510kreport.com/company/lifebridge-medizintechnik)
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)

## Its most-cited devices
- K052555: Medtronic Performer TM CPB, Model R51, PCPB (2006), cited by 2
- K120026: Performer HT/ Hang&GO HT Basic (2012), cited by 1
- K070213: Performer CBP System (2007), cited by 1

## Recent decisions
- K161613: Hang&Go PAC (Dec 28, 2016)
- K120026: Performer HT/ Hang&GO HT Basic (May 8, 2012)
- K070213: Performer CBP System (Mar 21, 2007)
- K052555: Medtronic Performer TM CPB, Model R51, PCPB (Mar 15, 2006)

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