OMRON DIGITAL BP MONITOR HEM-700CP
K-Number: K854201 · 1986-04-17
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Device Summary
Frequently Asked Questions
What is the OMRON DIGITAL BP MONITOR HEM-700CP?
OMRON DIGITAL BP MONITOR HEM-700CP is a medical device that received FDA 510(k) clearance on 1986-04-17. The listed applicant is Omron Tateisi Electronics Co.. The 510(k) number is K854201.
When did OMRON DIGITAL BP MONITOR HEM-700CP receive FDA 510(k) clearance?
OMRON DIGITAL BP MONITOR HEM-700CP received FDA 510(k) clearance on 1986-04-17, under 510(k) number K854201.
Who is the listed applicant for OMRON DIGITAL BP MONITOR HEM-700CP?
The FDA 510(k) record lists Omron Tateisi Electronics Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OMRON DIGITAL BP MONITOR HEM-700CP?
The FDA product code for OMRON DIGITAL BP MONITOR HEM-700CP 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 Tateisi Electronics Co. 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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