# Interson Corp.

- Location (FDA's records): Pleasanton, CA
- FDA decisions: 11 (1989–2023): 11 510(k) clearances
- Names in FDA's records: Interson Corp. (9); Interson Corporation (2)
- Product codes: ITX (6), IYN (2), FED (1), FCG (1), IYO (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 3 (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 whose devices it cites most
- Philips Healthcare, Inc.: 1 (https://510kreport.com/company/philips-healthcare)
- Regulatory Management Services: 1 (https://510kreport.com/company/regulatory-management-services)

## Firms that cite its devices most
- Dolphin Medical Imaging, LLC: 1 (https://510kreport.com/company/dolphin-medical-imaging)
- Emagine Solutions Technology, LLC: 1 (https://510kreport.com/company/emagine-solutions-technology)

## Its most-cited devices
- K163443: Interson USB Ultrasound System (2017), cited by 3

## Recent decisions
- K233734: Interson USB Ultrasound System (Dec 22, 2023)
- K163443: Interson USB Ultrasound System (Apr 13, 2017)
- K911116: Interson Endocavity Probe/Kontron Ultrasound Syst (Dec 20, 1991)
- K911117: Interson Endocavity Probe for Atl Ultrasound Syst (Dec 17, 1991)
- K911113: Interson Transrectal Probe/Kontron Ultrasound Syst (Dec 17, 1991)
- K911115: Interson Transrectal Probe/Atl Ultrasound System (Dec 17, 1991)
- K911114: Interson Endocavity Probe/Aloka Ultrasound System (Nov 19, 1991)
- K911464: Interson Disposable Biopsy Needle (Sep 27, 1991)

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