# Bentley Laboratories, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 55 (1976–1993): 55 510(k) clearances
- Product codes: DTZ (10), DTN (6), DTM (6), DRS (4), DXY (4), KRA (2), KRI (2), FJI (2), KDI (2), KRJ (2), DTR (2), FIQ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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 that cite its devices most
- Edwards Lifesciences, LLC: 1 (https://510kreport.com/company/edwards-lifesciences)
- Fresenius USA, Inc.: 1 (https://510kreport.com/company/fresenius-usa)
- Embol-X, Inc.: 1 (https://510kreport.com/company/embol-x)

## Its most-cited devices
- K820044: Arterial Blood Filter, #AF-1025 (1982), cited by 2
- K903641: Quick Prime Hemoconcen. NO. HQ-7000 and CBP-7000Q (1990), cited by 1

## Recent decisions
- K931967: HE-30 Gold (Jul 13, 1993)
- K913956: Blood Cardioplegia Heat Exchanger, Model #HE-30 (Jan 17, 1992)
- K913692: Venous Reservoir Bag Model NO. BMR-250(TM) (Nov 15, 1991)
- K903641: Quick Prime Hemoconcen. NO. HQ-7000 and CBP-7000Q (Nov 9, 1990)
- K894826: Univox W/Holders, Models Univox-HL, HLB, HLF (Feb 28, 1990)
- K874867: Catr (TM)-H Cardiotomy Holder (Feb 2, 1988)
- K874841: Integrated Membrane Oxygenator W/Cardiotomy Filter (Feb 2, 1988)
- K874618: Baxter Accuport (TM) Central Venous Catheter (Jan 19, 1988)

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