Sein Electronics Co., Ltd.
Sein Electronics Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 1991, most recent 2005.
Top product codes for Sein Electronics Co., Ltd.
Recent clearances by Sein Electronics Co., Ltd.
- K052108 — SEIN BLOOD GLUCOSE AND BLOOD PRESSURE MONITOR SYSTEM, MODEL BGP-100
- K042138 — FULL AUTO WRIST DIGITAL BLOOD PRESSURE MONITOR MODEL# SE-311
- K042014 — DIGITAL BLOOD PRESSURE MONITOR, MODELS SE-9000, SE-9200 AND SE-9400
- K032927 — FULL AUTO ARM DIGITAL BLOOD PRESSURE MONITOR
- K012054 — FULL AUTO WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL SE-312
- K003711 — AMBULATORY BLOOD PRESSURE MONITORING SYSTEM, MODEL SE-25M/25P
- K003282 — FULL AUTO BLOOD PRESSURE MONITOR, MODEL SE-7700H
- K991397 — TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR SE-30 TENS
- K973078 — WRIST BLOOD PRESSURE METER MODEL SE-330
- K952826 — FULL AUTO FUZZY BLOOD PRESSURE METER MODEL SE-7000
- K952827 — FULL AUTO WRIST BLOOD PRESSURE METER MODEL SE-5000
- K912588 — AUTOMATIC DIGITAL BLOOD PRESSURE METERS, MODELS
Data sourced from openFDA. This site is unofficial and independent of the FDA.