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FDA 510(k)

TAKEDA MEDICAL AUTO. AMBU. BLOOD PRESS. METER/2420

K-Number: K880079 · 1988-03-31

ApplicantA&D Engineering, Inc.
Decision Date1988-03-31
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TAKEDA MEDICAL AUTO. AMBU. BLOOD PRESS. METER/2420 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 1988-03-31 under 510(k) number K880079. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAKEDA MEDICAL AUTO. AMBU. BLOOD PRESS. METER/2420?

TAKEDA MEDICAL AUTO. AMBU. BLOOD PRESS. METER/2420 is a medical device that received FDA 510(k) clearance on 1988-03-31. The listed applicant is A&D Engineering, Inc.. The 510(k) number is K880079.

When did TAKEDA MEDICAL AUTO. AMBU. BLOOD PRESS. METER/2420 receive FDA 510(k) clearance?

TAKEDA MEDICAL AUTO. AMBU. BLOOD PRESS. METER/2420 received FDA 510(k) clearance on 1988-03-31, under 510(k) number K880079.

Who is the listed applicant for TAKEDA MEDICAL AUTO. AMBU. BLOOD PRESS. METER/2420?

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. AMBU. BLOOD PRESS. METER/2420?

The FDA product code for TAKEDA MEDICAL AUTO. AMBU. BLOOD PRESS. METER/2420 is DSK.

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Related Devices (Code: DSK)

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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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