# Citizen Watch Co., Ltd.

- Location (FDA's records): Washington, DC
- FDA decisions: 8 (1991–2006): 8 510(k) clearances
- Product codes: DXN (8)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (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 whose devices it cites most
- Omron Electronics, Inc.: 1 (https://510kreport.com/company/omron-electronics)

## Recent decisions
- K061161: Blood Pressure Meter, Model CH-311B (Jun 26, 2006)
- K052046: Blood Pressure Meter, Model CH-432 (Oct 19, 2005)
- K001244: Blood Pressure Meter, Models CH-631B, CH-631D, CH-632B, CH-632D (Sep 26, 2000)
- K984223: Blood Pressure Meter, Models CH-491, CH-481, CH-471 (Apr 28, 1999)
- K973061: CH-601A and CH-601B Digital Wrist Sphygmomanometer (CH-601A/CH-601B) (Mar 13, 1998)
- K954547: CH-502A & CH520B Digital Finger Sphygmomanometer (Apr 1, 1997)
- K923344: Electronic Digital Blood Pressure Monitor (Oct 7, 1993)
- K911965: Electronic Digital Blood Pressure/Pulse Monitor (Oct 28, 1991)

Source page: https://510kreport.com/company/citizen-watch