# Gould, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 31 (1976–1991): 31 510(k) clearances
- Product codes: DRS (6), DXG (4), KRB (4), DRT (3), DQO (2), DYG (2), DXN (1), DYB (1), CCK (1), DXJ (1), DRR (1), BZG (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 7 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Biosensors International-USA: 1 (https://510kreport.com/company/biosensors-international-usa)

## Its most-cited devices
- K830523: Catheter Connection W/Integral Injectate (1983), cited by 1

## Recent decisions
- K911935: Cardiac Electrophysical Lead Selector, Modified (Jul 22, 1991)
- K861092: Model SP1465 Cardiac Output Computer (Aug 18, 1986)
- K860805: Pressure Monitor Cath Models SP5325,SP5327,SP5337 (May 8, 1986)
- K855145: Model:TA-Rose Resonant Overshoot Eliminator (Feb 26, 1986)
- K854403: Model 2120 Spiroscreen (Jan 14, 1986)
- K851486: Gould Disposable Transducer & Accessories-DTX (Oct 17, 1985)
- K850114: C/Pes 9201, Ecg Stress Testing Sys (Feb 22, 1985)
- K850113: C/Pes 9103, Ecg Stress Testing System (Feb 8, 1985)

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