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FDA 510(k)

DIGITAL BLOOD PRESSURE MONITOR, MODELS HD-503 AND HD-505

K-Number: K002722 · 2000-09-11

ApplicantJawon Medical Co., Ltd.
Decision Date2000-09-11
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DIGITAL BLOOD PRESSURE MONITOR, MODELS HD-503 AND HD-505 is the device name listed in this FDA 510(k) record. The listed applicant is Jawon Medical Co., Ltd.. It received FDA 510(k) clearance on 2000-09-11 under 510(k) number K002722. 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 DIGITAL BLOOD PRESSURE MONITOR, MODELS HD-503 AND HD-505?

DIGITAL BLOOD PRESSURE MONITOR, MODELS HD-503 AND HD-505 is a medical device that received FDA 510(k) clearance on 2000-09-11. The listed applicant is Jawon Medical Co., Ltd.. The 510(k) number is K002722.

When did DIGITAL BLOOD PRESSURE MONITOR, MODELS HD-503 AND HD-505 receive FDA 510(k) clearance?

DIGITAL BLOOD PRESSURE MONITOR, MODELS HD-503 AND HD-505 received FDA 510(k) clearance on 2000-09-11, under 510(k) number K002722.

Who is the listed applicant for DIGITAL BLOOD PRESSURE MONITOR, MODELS HD-503 AND HD-505?

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

What is the FDA product code for DIGITAL BLOOD PRESSURE MONITOR, MODELS HD-503 AND HD-505?

The FDA product code for DIGITAL BLOOD PRESSURE MONITOR, MODELS HD-503 AND HD-505 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 Jawon Medical 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.

K092432AUTOMOATIC BLOOD PRESSURE MONITOR, MODELS: EASY X 800 AND 900 (R/L)K092431BODY COMPOSITION ANALYZER, MODEL: IOI 353K072325BODY COMPOSITION ANALYZER, EASYBODY 202, 203, 205K071884BODY COMPOSITION ANALYZER, MODELS: X-SCAN PLUS II, GAIA 359 PLUS, PLUSAVIS 333, XBIA 500, XBIA 900K062462NON-INVASIVE BLOOD PRESSURE MONITOR, MODELS FT-500R/L AND FT-700R/LK053556BODY COMPOSITION ANALYZER, MODELS ZEUS 9.9 AND VENUS 5.5

View all 11 devices →

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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