# Qisda Corporation

- Location (FDA's records): Taoyuan City, TW
- FDA decisions: 4 (2014–2019): 4 510(k) clearances
- Product codes: IYN (3), IYO (1)
- 510(k) review time since 2016: median 102 days, against 79 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 7 (3 its own); citations of its devices by later devices: 3 (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
- Philips Health Care: 2 (https://510kreport.com/company/philips-health-care)
- Chang Gung Medical Technology Co., Ltd. Linkou Fac: 1 (https://510kreport.com/company/chang-gung-medical-technology-co-linkou-fac)
- General Electric Co.: 1 (https://510kreport.com/company/general-electric)

## Its most-cited devices
- K181313: BenQ Diagnostic Ultrasound System (2018), cited by 1
- K132690: UP600 Diagnostic Doppler Ultrasound System (2014), cited by 1
- K172056: InnoSight Diagnostic Ultrasound System (2017), cited by 1

## Recent decisions
- K192254: InnoSight Diagnostic Ultrasound System (Sep 18, 2019)
- K181313: BenQ Diagnostic Ultrasound System (Aug 27, 2018)
- K172056: InnoSight Diagnostic Ultrasound System (Dec 13, 2017)
- K132690: UP600 Diagnostic Doppler Ultrasound System (Feb 25, 2014)

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