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FDA 510(k)

MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR

K-Number: K030221 · 2003-07-25

ApplicantMytech Technology Co., Ltd.
Decision Date2003-07-25
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Mytech Technology Co., Ltd.. It received FDA 510(k) clearance on 2003-07-25 under 510(k) number K030221. 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 MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR?

MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 2003-07-25. The listed applicant is Mytech Technology Co., Ltd.. The 510(k) number is K030221.

When did MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR receive FDA 510(k) clearance?

MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR received FDA 510(k) clearance on 2003-07-25, under 510(k) number K030221.

Who is the listed applicant for MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR?

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?

The FDA product code for MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR 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.

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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.

K061959MYTECH / HAPPY LIFE / MAXIAIDS ARM BLOOD PRESSURE MONITOR, HPL-301, HPL-302, HPL-310, 180310K041228MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODEL HPL-200K030561MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODELS HPL-100 AND HPL-100A

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

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

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