COPAL DIGITAL SPHYGMOMAMOMETER UA-550
K-Number: K844285 · 1985-04-18
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Device Summary
Frequently Asked Questions
What is the COPAL DIGITAL SPHYGMOMAMOMETER UA-550?
COPAL DIGITAL SPHYGMOMAMOMETER UA-550 is a medical device that received FDA 510(k) clearance on 1985-04-18. The listed applicant is Takeda Medical, Inc.. The 510(k) number is K844285.
When did COPAL DIGITAL SPHYGMOMAMOMETER UA-550 receive FDA 510(k) clearance?
COPAL DIGITAL SPHYGMOMAMOMETER UA-550 received FDA 510(k) clearance on 1985-04-18, under 510(k) number K844285.
Who is the listed applicant for COPAL DIGITAL SPHYGMOMAMOMETER UA-550?
The FDA 510(k) record lists Takeda Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COPAL DIGITAL SPHYGMOMAMOMETER UA-550?
The FDA product code for COPAL DIGITAL SPHYGMOMAMOMETER UA-550 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 Takeda Medical, 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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