# Non-Invasive Monitoring Systems, Inc.

- Location (FDA's records): Arlington, VA
- FDA decisions: 6 (1989–2001): 6 510(k) clearances
- Product codes: DQK (4), BZQ (1), BZK (1)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 6 (1 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
- Vivometrics, Inc.: 2 (https://510kreport.com/company/vivometrics)
- Carefusion Germany 234 GmbH: 1 (https://510kreport.com/company/carefusion-germany-234)
- Nox Medical Ehf: 1 (https://510kreport.com/company/nox-medical)
- Maquet Critical Care AB: 1 (https://510kreport.com/company/maquet-critical-care)

## Its most-cited devices
- K942852: Respitrace PT (1996), cited by 2
- K001369: Respievents, Version 4.2 (2000), cited by 2
- K012020: Respievents Software IS Event Data Processing Sofware for a PC (2001), cited by 1
- K903011: Respitrace Plus, Respibands, and Respicentral (1991), cited by 1

## Recent decisions
- K012020: Respievents Software IS Event Data Processing Sofware for a PC (Aug 21, 2001)
- K001369: Respievents, Version 4.2 (Jul 26, 2000)
- K942852: Respitrace PT (Feb 13, 1996)
- K942771: Respievents (Feb 13, 1996)
- K903011: Respitrace Plus, Respibands, and Respicentral (Mar 29, 1991)
- K884959: Respitrak (Jun 8, 1989)

Source page: https://510kreport.com/company/non-invasive-monitoring-systems