# Karmelsonix

- Location (FDA's records): Binyamina, IL
- FDA decisions: 4 (2007–2011): 4 510(k) clearances
- Product codes: BZM (3), DSH (1)
- Predicates its devices cite: 7 (3 its own); citations of its devices by later devices: 5 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Vasomedical, Inc.: 1 (https://510kreport.com/company/vasomedical)
- Stethographics, Inc.: 1 (https://510kreport.com/company/stethographics)
- Hospira, Inc.: 1 (https://510kreport.com/company/hospira)
- Karmel Medical Acoustic Technologies, Ltd.: 1 (https://510kreport.com/company/karmel-medical-acoustic-technologies)

## Firms that cite its devices most
- Vitalograph (Ireland), Ltd.: 1 (https://510kreport.com/company/vitalograph-ireland)
- Isonea, Ltd.: 1 (https://510kreport.com/company/isonea)

## Its most-cited devices
- K071955: Wim-PC, Model 1010 (2007), cited by 3
- K101022: Pulmotrack 5050 Wholter, Model 5050 (2010), cited by 1
- K090863: Personal Wheezometer (2009), cited by 1

## Recent decisions
- K102229: Pulmotrack 2020 System (Mar 4, 2011)
- K101022: Pulmotrack 5050 Wholter, Model 5050 (Jul 9, 2010)
- K090863: Personal Wheezometer (Sep 21, 2009)
- K071955: Wim-PC, Model 1010 (Nov 1, 2007)

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