# American Bentley

- Location (FDA's records): Irvine, CA
- FDA decisions: 59 (1983–1988): 59 510(k) clearances
- Product codes: DTZ (13), DTN (11), KRI (7), DTM (5), DTR (4), DRS (3), CCE (3), GEI (2), DWF (2), DTP (2), DTL (1), CCC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K872896: Umbilical Artery Oxygen Probe Model Uap-100 (Feb 12, 1988)
- K873923: Integrated Membrane Oxygenator W/Cardiotomy Filter (Nov 6, 1987)
- K870804: Cardioplegia Heat Exchanger Model NO. HE-100 (Sep 1, 1987)
- K872167: Cardiotomy/Mediastinal Auto. Reservoir Catr-3500 (Sep 1, 1987)
- K872133: Oxygenator Model NO. Bentley 5 Plus (Aug 24, 1987)
- K870911: Indwelling Blood Carbondioxide Partial Pres. Analy (May 29, 1987)
- K870269: Electrosurgical Meniscus Cutter (Emc) Mod. Amc-100 (Mar 9, 1987)
- K863249: Oxygenator Model NO. Bentley-10 Plus (Oct 20, 1986)

Source page: https://510kreport.com/company/american-bentley