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FDA 510(k)

MPV-7201 NON-INVASIVE BLOOD PRESSURE MONITOR

K-Number: K854370 · 1986-04-28

ApplicantNihon Kohden America, Inc.
Decision Date1986-04-28
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MPV-7201 NON-INVASIVE BLOOD PRESSURE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Kohden America, Inc.. It received FDA 510(k) clearance on 1986-04-28 under 510(k) number K854370. 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 MPV-7201 NON-INVASIVE BLOOD PRESSURE MONITOR?

MPV-7201 NON-INVASIVE BLOOD PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1986-04-28. The listed applicant is Nihon Kohden America, Inc.. The 510(k) number is K854370.

When did MPV-7201 NON-INVASIVE BLOOD PRESSURE MONITOR receive FDA 510(k) clearance?

MPV-7201 NON-INVASIVE BLOOD PRESSURE MONITOR received FDA 510(k) clearance on 1986-04-28, under 510(k) number K854370.

Who is the listed applicant for MPV-7201 NON-INVASIVE BLOOD PRESSURE MONITOR?

The FDA 510(k) record lists Nihon Kohden America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MPV-7201 NON-INVASIVE BLOOD PRESSURE MONITOR?

The FDA product code for MPV-7201 NON-INVASIVE BLOOD PRESSURE MONITOR is DXN.

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Other records listing Nihon Kohden America, Inc. as applicant

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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

View on FDA Database →

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

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