# Cerner Corp.

- Location (FDA's records): Kansas City, MO
- FDA decisions: 8 (1996–2015): 8 510(k) clearances
- Names in FDA's records: Cerner Corp. (7); Cerner Corporation (1)
- Product codes: LLZ (3), HGM (2), MSX (1), DRG (1), LMD (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 1 (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
- Airstrip Technologies, LP: 1 (https://510kreport.com/company/airstrip-technologies)

## Firms that cite its devices most
- Airstrip Technologies, LP: 1 (https://510kreport.com/company/airstrip-technologies)

## Its most-cited devices
- K093134: Cerner Careaware Ibus (2009), cited by 1

## Recent decisions
- K151672: Cerner CareAware Event Management (Dec 21, 2015)
- K121758: Cerner Fetalink+(VERSION1.0) (Oct 9, 2012)
- K093134: Cerner Careaware Ibus (Nov 27, 2009)
- K091251: Cerner Fetalink (Version 1.0) (Aug 25, 2009)
- K091032: Cerner Provision Workstation (Version 2.5) (Jun 22, 2009)
- K070394: Cerner Provision Workstation (Mar 27, 2007)
- K000770: Proview Medical Image Display Module (May 16, 2000)
- K955000: Remote Viewing System Medical Image Display Module (Jan 26, 1996)

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