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FDA 510(k)

TAKEDA MEDICAL DIGITAL SPHYGMOMANOMETER, UA-731

K-Number: K854797 · 1986-05-09

ApplicantTakeda Medical, Inc.
Decision Date1986-05-09
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TAKEDA MEDICAL DIGITAL SPHYGMOMANOMETER, UA-731 is the device name listed in this FDA 510(k) record. The listed applicant is Takeda Medical, Inc.. It received FDA 510(k) clearance on 1986-05-09 under 510(k) number K854797. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAKEDA MEDICAL DIGITAL SPHYGMOMANOMETER, UA-731?

TAKEDA MEDICAL DIGITAL SPHYGMOMANOMETER, UA-731 is a medical device that received FDA 510(k) clearance on 1986-05-09. The listed applicant is Takeda Medical, Inc.. The 510(k) number is K854797.

When did TAKEDA MEDICAL DIGITAL SPHYGMOMANOMETER, UA-731 receive FDA 510(k) clearance?

TAKEDA MEDICAL DIGITAL SPHYGMOMANOMETER, UA-731 received FDA 510(k) clearance on 1986-05-09, under 510(k) number K854797.

Who is the listed applicant for TAKEDA MEDICAL DIGITAL SPHYGMOMANOMETER, UA-731?

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 TAKEDA MEDICAL DIGITAL SPHYGMOMANOMETER, UA-731?

The FDA product code for TAKEDA MEDICAL DIGITAL SPHYGMOMANOMETER, UA-731 is DXN.

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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.

K853158DIGITAL SPHYGMOMANOMETER MODEL 7620K851223COPAL DIGITAL SPHYGMOMANOMETER UA-560K852564COPAL UA-512 DIGITAL BLOOD PRESSURE MONITORK843390COPAL DIGITAL SPHYGMOMANOMETER UA-535K844285COPAL DIGITAL SPHYGMOMAMOMETER UA-550K842388COPAL DIGITAL SPHYGMOMANOMETER UA-510

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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.

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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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