# Bracco Injeneering

- Location (FDA's records): Lausanne, CH
- FDA decisions: 2 (2014–2016): 2 510(k) clearances
- Names in FDA's records: Bracco Injeneering (1); Bracco Injeneering S.A. (1)
- Product codes: IZQ (1), PQH (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 4 (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
- Swiss Medical Care S.A.: 1 (https://510kreport.com/company/swiss-medical-care)
- E-Z-Em, Inc.: 1 (https://510kreport.com/company/e-z-em)

## Firms that cite its devices most
- Ulrich GmbH & Co. KG: 2 (https://510kreport.com/company/ulrich)
- Bayer U.S., LLC: 1 (https://510kreport.com/company/bayer-us)
- Imaxeon Pty, Ltd.: 1 (https://510kreport.com/company/imaxeon)

## Its most-cited devices
- K151048: CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set (2016), cited by 2
- K133147: Bracco Injeenering Transfer Set (2014), cited by 2

## Recent decisions
- K151048: CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set (Jan 22, 2016)
- K133147: Bracco Injeenering Transfer Set (Jun 20, 2014)

Source page: https://510kreport.com/company/bracco-injeneering