MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODEL HPL-200
K-Number: K041228 · 2004-05-17
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Device Summary
Frequently Asked Questions
What is the MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODEL HPL-200?
MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODEL HPL-200 is a medical device that received FDA 510(k) clearance on 2004-05-17. The listed applicant is Mytech Technology Co., Ltd.. The 510(k) number is K041228.
When did MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODEL HPL-200 receive FDA 510(k) clearance?
MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODEL HPL-200 received FDA 510(k) clearance on 2004-05-17, under 510(k) number K041228.
Who is the listed applicant for MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODEL HPL-200?
The FDA 510(k) record lists Mytech Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODEL HPL-200?
The FDA product code for MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODEL HPL-200 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 Mytech Technology 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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