# Bayer Corp., Agfa Div.

- Location (FDA's records): Ridgefield Park, NJ
- FDA decisions: 3 (1997–1998): 3 510(k) clearances
- Product codes: IXW (1), LMC (1), KPR (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 7 (0 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
- Enhanced Imaging Technologies, Inc.: 1 (https://510kreport.com/company/enhanced-imaging-technologies)

## Firms that cite its devices most
- Agfa Corp.: 3 (https://510kreport.com/company/agfa)
- Alara, Inc.: 2 (https://510kreport.com/company/alara)
- Imation Enterprises Corp.: 1 (https://510kreport.com/company/imation-enterprises)
- Agfa-Gevaert, Inc.: 1 (https://510kreport.com/company/agfa-gevaert)

## Its most-cited devices
- K974597: Adc Compact (Agfa Diagnostic Center) (1998), cited by 4
- K964414: LR 5200 Laser Film Recorder (1997), cited by 3

## Recent decisions
- K981280: CP 1000, Curix HT 330, Classic E.O.S., Curix HT 530, Mamoray HT 300, Mamoray Cmpact Plus, Curix Compact Plus, Curix Coms (Apr 30, 1998)
- K974597: Adc Compact (Agfa Diagnostic Center) (Mar 9, 1998)
- K964414: LR 5200 Laser Film Recorder (Jan 27, 1997)

Source page: https://510kreport.com/company/bayer-agfa-div