AUTO DIGITAL UPPER ARM BLOOD PRESSURE MONITOR, MODEL KP-7770
K-Number: K092806 · 2009-10-09
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Device Summary
Frequently Asked Questions
What is the AUTO DIGITAL UPPER ARM BLOOD PRESSURE MONITOR, MODEL KP-7770?
AUTO DIGITAL UPPER ARM BLOOD PRESSURE MONITOR, MODEL KP-7770 is a medical device that received FDA 510(k) clearance on 2009-10-09. The listed applicant is K-Jump Health Co., Ltd.. The 510(k) number is K092806.
When did AUTO DIGITAL UPPER ARM BLOOD PRESSURE MONITOR, MODEL KP-7770 receive FDA 510(k) clearance?
AUTO DIGITAL UPPER ARM BLOOD PRESSURE MONITOR, MODEL KP-7770 received FDA 510(k) clearance on 2009-10-09, under 510(k) number K092806.
Who is the listed applicant for AUTO DIGITAL UPPER ARM BLOOD PRESSURE MONITOR, MODEL KP-7770?
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 AUTO DIGITAL UPPER ARM BLOOD PRESSURE MONITOR, MODEL KP-7770?
The FDA product code for AUTO DIGITAL UPPER ARM BLOOD PRESSURE MONITOR, MODEL KP-7770 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.
Other records listing K-Jump Health 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.
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.
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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