DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL LD 1143
K-Number: K092683 · 2009-09-25
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Device Summary
Frequently Asked Questions
What is the DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL LD 1143?
DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL LD 1143 is a medical device that received FDA 510(k) clearance on 2009-09-25. The listed applicant is Shanghai Little Doctor Co. Limited. The 510(k) number is K092683.
When did DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL LD 1143 receive FDA 510(k) clearance?
DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL LD 1143 received FDA 510(k) clearance on 2009-09-25, under 510(k) number K092683.
Who is the listed applicant for DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL LD 1143?
The FDA 510(k) record lists Shanghai Little Doctor Co. Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL LD 1143?
The FDA product code for DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL LD 1143 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.
Other records listing Shanghai Little Doctor Co. Limited 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.
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.
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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