AMBULATORY BLOOD PRESSURE MONITOR, MODELS FB-270 AND DS-270
K-Number: K093102 · 2010-06-03
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Device Summary
Frequently Asked Questions
What is the AMBULATORY BLOOD PRESSURE MONITOR, MODELS FB-270 AND DS-270?
AMBULATORY BLOOD PRESSURE MONITOR, MODELS FB-270 AND DS-270 is a medical device that received FDA 510(k) clearance on 2010-06-03. The listed applicant is Nihon Seimitsu Sokki Co., Ltd.. The 510(k) number is K093102.
When did AMBULATORY BLOOD PRESSURE MONITOR, MODELS FB-270 AND DS-270 receive FDA 510(k) clearance?
AMBULATORY BLOOD PRESSURE MONITOR, MODELS FB-270 AND DS-270 received FDA 510(k) clearance on 2010-06-03, under 510(k) number K093102.
Who is the listed applicant for AMBULATORY BLOOD PRESSURE MONITOR, MODELS FB-270 AND DS-270?
The FDA 510(k) record lists Nihon Seimitsu Sokki Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AMBULATORY BLOOD PRESSURE MONITOR, MODELS FB-270 AND DS-270?
The FDA product code for AMBULATORY BLOOD PRESSURE MONITOR, MODELS FB-270 AND DS-270 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 Nihon Seimitsu Sokki 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.
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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