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FDA 510(k)

TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR

K-Number: K882824 · 1989-01-17

Decision Date1989-01-17
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is A&D Engineering, Inc.. It received FDA 510(k) clearance on 1989-01-17 under 510(k) number K882824. 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 AUTO. DIGITAL BLOOD PRES. MONITOR?

TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR is a medical device that received FDA 510(k) clearance on 1989-01-17. The listed applicant is A&D Engineering, Inc.. The 510(k) number is K882824.

When did TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR receive FDA 510(k) clearance?

TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR received FDA 510(k) clearance on 1989-01-17, under 510(k) number K882824.

Who is the listed applicant for TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR?

The FDA 510(k) record lists A&D Engineering, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR?

The FDA product code for TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR 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 A&D Engineering, 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.

View all 34 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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