DIGITAL BLOOD PRESSURE MONITOR, MODELS HD-503 AND HD-505— 510(k) K002722

Substantially Equivalent

Jawon Medical Co., Ltd.

FDA 510(k) clearance K002722 for DIGITAL BLOOD PRESSURE MONITOR, MODELS HD-503 AND HD-505, Substantially Equivalent on 2000-09-11. Applicant: Jawon Medical Co., Ltd..

Clearance details

Applicant: Jawon Medical Co., Ltd.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2000-08-31
Decision date: 2000-09-11
Decision: Substantially Equivalent
Clearance type: Special
Location: Seoul, KR

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Adverse events under product code DXN

product code DXN

Death: 3
Injury: 169
Malfunction: 1,019
Other: 2
Total: 1,193

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.