# Dalian Labtek Science & Development Co., Ltd.

- Location (FDA's records): Shanghai, CN
- FDA decisions: 3 (2012–2022): 3 510(k) clearances
- Product codes: JOW (3)
- Predicates its devices cite: 2 (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
- Daesung Maref Co., Ltd.: 1 (https://510kreport.com/company/daesung-maref)

## Firms that cite its devices most
- Wuhan Landing Medical Hi-Tech, Ltd.: 1 (https://510kreport.com/company/wuhan-landing-medical-hi-tech)

## Its most-cited devices
- K123830: Intermittent Pneumatic Compression Device (2013), cited by 2

## Recent decisions
- K213313: Veinoflow SCD (Model: LBTK-M-I 5006) (Feb 9, 2022)
- K123830: Intermittent Pneumatic Compression Device (Aug 16, 2013)
- K121718: A-V Foot Pump (Aug 17, 2012)

Source page: https://510kreport.com/company/dalian-labtek-science-development