# Dynatech/Nevada, Inc.

- Location (FDA's records): Carson City, NV
- FDA decisions: 6 (1990–1995): 6 510(k) clearances
- Product codes: DRT (1), DRL (1), FRN (1), DPS (1), DSI (1), DXN (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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
- Bio-Tek Instruments, Inc.: 2 (https://510kreport.com/company/bio-tek-instruments)
- Fluke Biomedical: 1 (https://510kreport.com/company/fluke-biomedical)
- Datrend Systems, Inc.: 1 (https://510kreport.com/company/datrend-systems)

## Its most-cited devices
- K897096: Model 404A I.V. Infusion Pump Analyzer (1990), cited by 3
- K935817: Medsim 300 Patient Simulator (1994), cited by 1

## Recent decisions
- K942546: Cufflink Non-Invasive Blood Pressure Analyzer (Jan 27, 1995)
- K935817: Medsim 300 Patient Simulator (Jan 18, 1994)
- K934254: Impulse 3000 Defibrillator Analyzer (Nov 23, 1993)
- K897074: Model 215M Patient Simulator (May 17, 1990)
- K897029: Model ECG100 Simulator (Apr 26, 1990)
- K897096: Model 404A I.V. Infusion Pump Analyzer (Mar 15, 1990)

Source page: https://510kreport.com/company/dynatech-nevada