DIGITAL BLOOD PRESSURE MONITOR MODEL HEM-703CP
K-Number: K882393 · 1988-08-30
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Device Summary
Frequently Asked Questions
What is the DIGITAL BLOOD PRESSURE MONITOR MODEL HEM-703CP?
DIGITAL BLOOD PRESSURE MONITOR MODEL HEM-703CP is a medical device that received FDA 510(k) clearance on 1988-08-30. The listed applicant is Omron Electronics, Inc.. The 510(k) number is K882393.
When did DIGITAL BLOOD PRESSURE MONITOR MODEL HEM-703CP receive FDA 510(k) clearance?
DIGITAL BLOOD PRESSURE MONITOR MODEL HEM-703CP received FDA 510(k) clearance on 1988-08-30, under 510(k) number K882393.
Who is the listed applicant for DIGITAL BLOOD PRESSURE MONITOR MODEL HEM-703CP?
The FDA 510(k) record lists Omron Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIGITAL BLOOD PRESSURE MONITOR MODEL HEM-703CP?
The FDA product code for DIGITAL BLOOD PRESSURE MONITOR MODEL HEM-703CP 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 Omron Electronics, Inc. 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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