# Amcad Biomed Corporation

- Location (FDA's records): Taipei, TW
- FDA decisions: 5 (2017–2021): 5 510(k) clearances
- Product codes: LLZ (4), QIH (1)
- 510(k) review time since 2016: median 257 days, against 107 for FDA's reviews in the same codes and years (0 of 5 faster)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 2 (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
- Edda Technology, Inc.: 1 (https://510kreport.com/company/edda-technology)
- Philips Ultrasound, Inc.: 1 (https://510kreport.com/company/philips-ultrasound)
- Lin & Associates, LLC: 1 (https://510kreport.com/company/lin-associates)
- Advanced Technology Laboratories, Inc.: 1 (https://510kreport.com/company/advanced-technology-laboratories)

## Firms that cite its devices most
- Piur Imaging GmbH: 1 (https://510kreport.com/company/piur-imaging)

## Its most-cited devices
- K180006: AmCAD-UT Detection 2.2 (2018), cited by 1
- K203555: AmCAD-UT (2021), cited by 1

## Recent decisions
- K203555: AmCAD-UT (Sep 8, 2021)
- K180867: AmCAD-UO (Dec 28, 2018)
- K180006: AmCAD-UT Detection 2.2 (Aug 31, 2018)
- K162574: AmCAD-US (May 30, 2017)
- K170069: AmCAD-UV (Apr 26, 2017)

Source page: https://510kreport.com/company/amcad-biomed