BLOOD PRESSURE MONITOR SMARTLOGIC, MODELS KP-6210 AND KP-6211
K-Number: K022916 · 2002-11-21
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Device Summary
Frequently Asked Questions
What is the BLOOD PRESSURE MONITOR SMARTLOGIC, MODELS KP-6210 AND KP-6211?
BLOOD PRESSURE MONITOR SMARTLOGIC, MODELS KP-6210 AND KP-6211 is a medical device that received FDA 510(k) clearance on 2002-11-21. The listed applicant is K-Jump Health Co., Ltd.. The 510(k) number is K022916.
When did BLOOD PRESSURE MONITOR SMARTLOGIC, MODELS KP-6210 AND KP-6211 receive FDA 510(k) clearance?
BLOOD PRESSURE MONITOR SMARTLOGIC, MODELS KP-6210 AND KP-6211 received FDA 510(k) clearance on 2002-11-21, under 510(k) number K022916.
Who is the listed applicant for BLOOD PRESSURE MONITOR SMARTLOGIC, MODELS KP-6210 AND KP-6211?
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 SMARTLOGIC, MODELS KP-6210 AND KP-6211?
The FDA product code for BLOOD PRESSURE MONITOR SMARTLOGIC, MODELS KP-6210 AND KP-6211 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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