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FDA 510(k)

WRIST TYPE DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-303S

K-Number: K991688 · 1999-06-01

ApplicantJawon Medical Co., Ltd.
Decision Date1999-06-01
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WRIST TYPE DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-303S 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 1999-06-01 under 510(k) number K991688. 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 WRIST TYPE DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-303S?

WRIST TYPE DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-303S is a medical device that received FDA 510(k) clearance on 1999-06-01. The listed applicant is Jawon Medical Co., Ltd.. The 510(k) number is K991688.

When did WRIST TYPE DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-303S receive FDA 510(k) clearance?

WRIST TYPE DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-303S received FDA 510(k) clearance on 1999-06-01, under 510(k) number K991688.

Who is the listed applicant for WRIST TYPE DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-303S?

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 WRIST TYPE DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-303S?

The FDA product code for WRIST TYPE DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-303S is DXN.

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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

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Related Devices (Code: DXN)

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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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