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FDA 510(k)

BLOOD PRESSURE MONITOR, MODELS BP-102, BP-103, BP-201 AND BP-202

K-Number: K080789 · 2008-04-03

ApplicantSejoy Electronics & Instruments Co., Ltd.
Decision Date2008-04-03
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BLOOD PRESSURE MONITOR, MODELS BP-102, BP-103, BP-201 AND BP-202 is the device name listed in this FDA 510(k) record. The listed applicant is Sejoy Electronics & Instruments Co., Ltd.. It received FDA 510(k) clearance on 2008-04-03 under 510(k) number K080789. 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 BLOOD PRESSURE MONITOR, MODELS BP-102, BP-103, BP-201 AND BP-202?

BLOOD PRESSURE MONITOR, MODELS BP-102, BP-103, BP-201 AND BP-202 is a medical device that received FDA 510(k) clearance on 2008-04-03. The listed applicant is Sejoy Electronics & Instruments Co., Ltd.. The 510(k) number is K080789.

When did BLOOD PRESSURE MONITOR, MODELS BP-102, BP-103, BP-201 AND BP-202 receive FDA 510(k) clearance?

BLOOD PRESSURE MONITOR, MODELS BP-102, BP-103, BP-201 AND BP-202 received FDA 510(k) clearance on 2008-04-03, under 510(k) number K080789.

Who is the listed applicant for BLOOD PRESSURE MONITOR, MODELS BP-102, BP-103, BP-201 AND BP-202?

The FDA 510(k) record lists Sejoy Electronics & Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD PRESSURE MONITOR, MODELS BP-102, BP-103, BP-201 AND BP-202?

The FDA product code for BLOOD PRESSURE MONITOR, MODELS BP-102, BP-103, BP-201 AND BP-202 is DXN.

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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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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

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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