# Caird Technology

- Location (FDA's records): Columbia, SC
- FDA decisions: 3 (1998–2011): 3 510(k) clearances
- Product codes: DPS (2), BZG (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Welch Allyn, Inc.: 2 (https://510kreport.com/company/welch-allyn)
- Medikro OY: 2 (https://510kreport.com/company/medikro)
- Bionet Co., Ltd.: 1 (https://510kreport.com/company/bionet)
- Pulse Biomedical, Inc.: 1 (https://510kreport.com/company/pulse-biomedical)
- Rozinn Electronics, Inc.: 1 (https://510kreport.com/company/rozinn-electronics)

## Its most-cited devices
- K971336: Caird Technology Spirometer (1998), cited by 5
- K012686: Caird Technology Holter 2000 (2001), cited by 2

## Recent decisions
- K101016: Ans System (Jan 28, 2011)
- K012686: Caird Technology Holter 2000 (Dec 13, 2001)
- K971336: Caird Technology Spirometer (Dec 1, 1998)

Source page: https://510kreport.com/company/caird-technology