# Oldelft Corp. of America

- Location (FDA's records): Fairfax, VA
- FDA decisions: 9 (1989–1998): 9 510(k) clearances
- Product codes: KPQ (2), KPR (2), KQA (1), JAD (1), IZO (1), JAK (1), IZG (1)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 7 (2 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
- Rogan Imaging Corp.: 1 (https://510kreport.com/company/rogan-imaging)

## Firms that cite its devices most
- Nucletron Corp.: 3 (https://510kreport.com/company/nucletron)
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)
- Acceletronics Digital Imaging, LLC: 1 (https://510kreport.com/company/acceletronics-digital-imaging)

## Its most-cited devices
- K946128: Simulix-HP (1995), cited by 2
- K980296: Oldelft Digidelca (1998), cited by 1
- K912466: Oldelft Simulix-MC (1991), cited by 1
- K932848: Simulix-MC CT Extension (1994), cited by 1
- K892659: Electrodelca (1989), cited by 1
- K973219: Amber DU (1997), cited by 1

## Recent decisions
- K980296: Oldelft Digidelca (Apr 17, 1998)
- K973219: Amber DU (Oct 8, 1997)
- K946128: Simulix-HP (May 12, 1995)
- K950037: N 800 HF (Feb 15, 1995)
- K932848: Simulix-MC CT Extension (Mar 22, 1994)
- K923584: Therapax DXT 300 Series 3 (Jan 15, 1993)
- K914784: Papillion Proctoscope (Jun 5, 1992)
- K912466: Oldelft Simulix-MC (Jun 28, 1991)

Source page: https://510kreport.com/company/oldelft-of-america