Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

WRIST BLOOD PRESSURE MONITOR & FAT METER, MODEL WT-20

K-Number: K031582 · 2003-08-01

ApplicantNihon Seimitsu Sokki Co., Ltd.
Decision Date2003-08-01
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WRIST BLOOD PRESSURE MONITOR & FAT METER, MODEL WT-20 is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Seimitsu Sokki Co., Ltd.. It received FDA 510(k) clearance on 2003-08-01 under 510(k) number K031582. The device is classified under product code MNW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WRIST BLOOD PRESSURE MONITOR & FAT METER, MODEL WT-20?

WRIST BLOOD PRESSURE MONITOR & FAT METER, MODEL WT-20 is a medical device that received FDA 510(k) clearance on 2003-08-01. The listed applicant is Nihon Seimitsu Sokki Co., Ltd.. The 510(k) number is K031582.

When did WRIST BLOOD PRESSURE MONITOR & FAT METER, MODEL WT-20 receive FDA 510(k) clearance?

WRIST BLOOD PRESSURE MONITOR & FAT METER, MODEL WT-20 received FDA 510(k) clearance on 2003-08-01, under 510(k) number K031582.

Who is the listed applicant for WRIST BLOOD PRESSURE MONITOR & FAT METER, MODEL WT-20?

The FDA 510(k) record lists Nihon Seimitsu Sokki Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WRIST BLOOD PRESSURE MONITOR & FAT METER, MODEL WT-20?

The FDA product code for WRIST BLOOD PRESSURE MONITOR & FAT METER, MODEL WT-20 is MNW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Nihon Seimitsu Sokki Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K112620DISITAL BLOOD PRESSURE MONITORK112690BLOOD PRESSURE MONITORK112691BLOOD PRESSURE MONITORK093102AMBULATORY BLOOD PRESSURE MONITOR, MODELS FB-270 AND DS-270K080177WRIST BLOOD PRESSURE MONITOR, MODEL WS-1100/WS-1100PVK071596POTABLE AIR MASSAGER PUTIFINO, MODEL AM-7

View all 21 devices →

Related Devices (Code: MNW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K231116Multi-parameter detectorZhongshan Jinli Electronic Weighing Equipment Co., Ltd.K130856BIA / VITALITY ANALYZERIpgdx, LLCK130777INBODYBiospace Corporation LimitedK130952PRECISION ONE LIFECARE; DETECTO; DETECTOPrecision One Lifecare, Ltd.K131394TRANSTEK GLASS BODY FAT ANALYZERGuangdong Transtek Medical Electronics Co., Ltd.K130311TRANSTEK BODY FAT ANALYZERGuangdong Transtek Medical Electronics Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑