OMRON OSCILLOMETRIC DIGITAL BLOOD PRESSURE MONIT.
K-Number: K930798 · 1993-05-13
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Device Summary
Frequently Asked Questions
What is the OMRON OSCILLOMETRIC DIGITAL BLOOD PRESSURE MONIT.?
OMRON OSCILLOMETRIC DIGITAL BLOOD PRESSURE MONIT. is a medical device that received FDA 510(k) clearance on 1993-05-13. The listed applicant is Omron Healthcare, Inc.. The 510(k) number is K930798.
When did OMRON OSCILLOMETRIC DIGITAL BLOOD PRESSURE MONIT. receive FDA 510(k) clearance?
OMRON OSCILLOMETRIC DIGITAL BLOOD PRESSURE MONIT. received FDA 510(k) clearance on 1993-05-13, under 510(k) number K930798.
Who is the listed applicant for OMRON OSCILLOMETRIC DIGITAL BLOOD PRESSURE MONIT.?
The FDA 510(k) record lists Omron Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OMRON OSCILLOMETRIC DIGITAL BLOOD PRESSURE MONIT.?
The FDA product code for OMRON OSCILLOMETRIC DIGITAL BLOOD PRESSURE MONIT. 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 Healthcare, 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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