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FDA 510(k)

BLOOD PRESSURE MONITOR, MODEL KP-7000

K-Number: K032492 · 2003-09-09

ApplicantK-Jump Health Co., Ltd.
Decision Date2003-09-09
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BLOOD PRESSURE MONITOR, MODEL KP-7000 is the device name listed in this FDA 510(k) record. The listed applicant is K-Jump Health Co., Ltd.. It received FDA 510(k) clearance on 2003-09-09 under 510(k) number K032492. 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 BLOOD PRESSURE MONITOR, MODEL KP-7000?

BLOOD PRESSURE MONITOR, MODEL KP-7000 is a medical device that received FDA 510(k) clearance on 2003-09-09. The listed applicant is K-Jump Health Co., Ltd.. The 510(k) number is K032492.

When did BLOOD PRESSURE MONITOR, MODEL KP-7000 receive FDA 510(k) clearance?

BLOOD PRESSURE MONITOR, MODEL KP-7000 received FDA 510(k) clearance on 2003-09-09, under 510(k) number K032492.

Who is the listed applicant for BLOOD PRESSURE MONITOR, MODEL KP-7000?

The FDA 510(k) record lists K-Jump Health Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD PRESSURE MONITOR, MODEL KP-7000?

The FDA product code for BLOOD PRESSURE MONITOR, MODEL KP-7000 is DXN.

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Other records listing K-Jump Health Co., Ltd. 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.

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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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