# Omron Tateisi Electronics Co.

- Location (FDA's records): Tokyo, 105 Japan, JP
- FDA decisions: 7 (1985–1988): 7 510(k) clearances
- Product codes: DXN (5), DRS (1), CAF (1)
- Predicates its devices cite: 0 (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

## Recent decisions
- K881601: Omron Digital Blood Pressure Monitor Model HEM403C (Jun 15, 1988)
- K881602: Omron Digital Blood Pressure Monitor Model HEM703C (Jun 15, 1988)
- K871371: Digital Sphygmomanometer (Jun 12, 1987)
- K864466: Omron Ultrasonic Nebulizer Model NE-UO5 (Mar 26, 1987)
- K854201: Omron Digital BP Monitor Hem-700CP (Apr 17, 1986)
- K853260: Omron Digital BP Monitor Hem-700C (Nov 18, 1985)
- K851707: Omron Digital BP Monitor Hem-400C (Jul 31, 1985)

Source page: https://510kreport.com/company/omron-tateisi-electronics