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FDA 510(k)

GENTEEL WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL BP-100

K-Number: K022926 · 2003-06-06

ApplicantGenteel Technology Co., Ltd.
Decision Date2003-06-06
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GENTEEL WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL BP-100 is the device name listed in this FDA 510(k) record. The listed applicant is Genteel Technology Co., Ltd.. It received FDA 510(k) clearance on 2003-06-06 under 510(k) number K022926. 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 GENTEEL WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL BP-100?

GENTEEL WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL BP-100 is a medical device that received FDA 510(k) clearance on 2003-06-06. The listed applicant is Genteel Technology Co., Ltd.. The 510(k) number is K022926.

When did GENTEEL WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL BP-100 receive FDA 510(k) clearance?

GENTEEL WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL BP-100 received FDA 510(k) clearance on 2003-06-06, under 510(k) number K022926.

Who is the listed applicant for GENTEEL WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL BP-100?

The FDA 510(k) record lists Genteel Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GENTEEL WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL BP-100?

The FDA product code for GENTEEL WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL BP-100 is DXN.

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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.

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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