HEM-7200-Z (BP742)
K-Number: K121932 · 2012-08-29
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Device Summary
Frequently Asked Questions
What is the HEM-7200-Z (BP742)?
HEM-7200-Z (BP742) is a medical device that received FDA 510(k) clearance on 2012-08-29. The listed applicant is Omron Healthcare, Inc.. The 510(k) number is K121932.
When did HEM-7200-Z (BP742) receive FDA 510(k) clearance?
HEM-7200-Z (BP742) received FDA 510(k) clearance on 2012-08-29, under 510(k) number K121932.
Who is the listed applicant for HEM-7200-Z (BP742)?
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 HEM-7200-Z (BP742)?
The FDA product code for HEM-7200-Z (BP742) is DXN.
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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