Nihon Seimitsu Sokki Co., Ltd.
FDA 510(k) medical device clearances.
Top product codes for Nihon Seimitsu Sokki Co., Ltd.
Recent clearances by Nihon Seimitsu Sokki Co., Ltd.
- K112620 — DISITAL BLOOD PRESSURE MONITOR
- K112690 — BLOOD PRESSURE MONITOR
- K112691 — BLOOD PRESSURE MONITOR
- K093102 — AMBULATORY BLOOD PRESSURE MONITOR, MODELS FB-270 AND DS-270
- K080177 — WRIST BLOOD PRESSURE MONITOR, MODEL WS-1100/WS-1100PV
- K071596 — POTABLE AIR MASSAGER PUTIFINO, MODEL AM-7
- K071384 — MODIFICATION TO: DIGITAL BLOOD PRESSURE MONITOR, MODEL 1901
- K061086 — DM-3000 DIGITAL BLOOD PRESSURE MONITOR
- K050697 — MODEL DS-1901 DIGITAL BLOOD PRESSURE MONITOR
- K040309 — DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-1862
- K031582 — WRIST BLOOD PRESSURE MONITOR & FAT METER, MODEL WT-20
- K012194 — BLOOD PRESSURE MONITOR (SPHYGMOMANOMETER), MODEL HT-110
- K003444 — MODEL WS-500 DIGITAL WRIST BLOOD PRESSURE MONITOR
- K993890 — DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-181
- K981702 — AUTOMATIC DIGITAL ELECTRONIC WRIST BLOOD PRESSURE MONITOR MODEL NUMBER WS-300
- K952494 — DIGITAL ELECTRONIC WRIST BLOOD PRESSURE MONITOR
- K882635 — ELECTRONIC DIGITAL BLOOD PRESSURE MONITOR
- K850318 — UNISONIC ELECTRONIC DIGITAL BP MONITOR EMB-4050
- K850315 — UNISONIC ELECTRONIC DIGITAL BP MONITOR EBM-1050
- K850316 — UNISONIC ELECTRONIC DIGITAL BP MONITOR EBM-2050
- K850317 — UNISONIC ELECTRONIC DIGITAL BP MONITOR EBM-3050
Data sourced from openFDA. This site is unofficial and independent of the FDA.