# Verathon Incorporated

- Location (FDA's records): Bothell, WA
- FDA decisions: 5 (2007–2017): 5 510(k) clearances
- Product codes: IYO (5)
- Predicates its devices cite: 7 (4 its own); citations of its devices by later devices: 15 (4 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Diagnostic Ultrasound Corp.: 2 (https://510kreport.com/company/diagnostic-ultrasound)
- Sonosite,Inc.: 1 (https://510kreport.com/company/sonosite)

## Firms that cite its devices most
- Mcube Technology Co., Ltd.: 2 (https://510kreport.com/company/mcube-technology)
- Hoana Medical, Inc.: 2 (https://510kreport.com/company/hoana-medical)
- Mianyang Meike Electronic Equipment Co., Ltd.: 1 (https://510kreport.com/company/mianyang-meike-electronic-equipment)
- Vitacon Medical, Inc.: 1 (https://510kreport.com/company/vitacon-medical)
- Butterfly Network, Inc.: 1 (https://510kreport.com/company/butterfly-network)
- Lilium Otsuka Co., Ltd.: 1 (https://510kreport.com/company/lilium-otsuka)
- Edgecare, Inc.: 1 (https://510kreport.com/company/edgecare)
- Rivanna Medical, Inc.: 1 (https://510kreport.com/company/rivanna-medical)

## Its most-cited devices
- K071217: Bladderscan Bvi 9400 Ultrasound (2007), cited by 12
- K172356: BladderScan Prime PLUS System (2017), cited by 2
- K153101: BladderScan Prime System (2015), cited by 1

## Recent decisions
- K172356: BladderScan Prime PLUS System (Sep 15, 2017)
- K153101: BladderScan Prime System (Nov 19, 2015)
- K090214: Verathon Inc. Bladderscan BVM 9500 Ultrasound (Mar 13, 2009)
- K082456: Verathon Inc. Bladderscan Ultrasound System, Model Bvi 9600 (Dec 1, 2008)
- K071217: Bladderscan Bvi 9400 Ultrasound (May 17, 2007)

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