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FDA 510(k)

MARS DIGITAL BLOOD PRESSURE MONITOR

K-Number: K945215 · 1996-01-31

ApplicantMars Metal Co., Ltd.
Decision Date1996-01-31
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MARS DIGITAL BLOOD PRESSURE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Mars Metal Co., Ltd.. It received FDA 510(k) clearance on 1996-01-31 under 510(k) number K945215. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARS DIGITAL BLOOD PRESSURE MONITOR?

MARS DIGITAL BLOOD PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1996-01-31. The listed applicant is Mars Metal Co., Ltd.. The 510(k) number is K945215.

When did MARS DIGITAL BLOOD PRESSURE MONITOR receive FDA 510(k) clearance?

MARS DIGITAL BLOOD PRESSURE MONITOR received FDA 510(k) clearance on 1996-01-31, under 510(k) number K945215.

Who is the listed applicant for MARS DIGITAL BLOOD PRESSURE MONITOR?

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

What is the FDA product code for MARS DIGITAL BLOOD PRESSURE MONITOR?

The FDA product code for MARS DIGITAL BLOOD PRESSURE MONITOR is DXN.

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 Mars Metal 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.

K780715ANEROID TYPE BLOOD PRESSURE KIT

Related Devices (Code: DXN)

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.

K261929Upper Arm Blood pressure monitor (BP7155D)OMRON Healthcare, Inc.K254000Happy Health Blood Pressure MonitorHappy Health, Inc.K262658Automatic Digital Blood Pressure monitor (LD-526)Honsun (Nantong) Co., Ltd.K261394Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6186 Plus, DBP-6286B Plus, DBP-61E3 Plus, DBP-61E2 Plus, DBP-62E3B Plus, DBP-62E2B Plus)JOYTECH Healthcare Co., Ltd.K253425Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6194-P,DBP-6294B-P,DBP-6195P,DBP-6295B-P, DBP-6196P,DBP-6296B-P,DBP-61E1-P, DBP-62E1B-P,DBP-62E3B-P,DBP-61E2-P,DBP-62E2B-P,DBP-61E3-P,DBP-6173-P,DBP-6273B-P,DBP-6179-P,DBP-6279B-P)Joytech Healthcare Co. , Ltd.K261061BP Go (BPP-855)Wellvii, Inc.

Official Source

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

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