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FDA 510(k)

MODIFIED MODEL UA-751 DIGITAL SPHYGMONOMETER

K-Number: K871719 · 1987-06-05

ApplicantA&D Engineering, Inc.
Decision Date1987-06-05
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED MODEL UA-751 DIGITAL SPHYGMONOMETER 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 1987-06-05 under 510(k) number K871719. 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 MODIFIED MODEL UA-751 DIGITAL SPHYGMONOMETER?

MODIFIED MODEL UA-751 DIGITAL SPHYGMONOMETER is a medical device that received FDA 510(k) clearance on 1987-06-05. The listed applicant is A&D Engineering, Inc.. The 510(k) number is K871719.

When did MODIFIED MODEL UA-751 DIGITAL SPHYGMONOMETER receive FDA 510(k) clearance?

MODIFIED MODEL UA-751 DIGITAL SPHYGMONOMETER received FDA 510(k) clearance on 1987-06-05, under 510(k) number K871719.

Who is the listed applicant for MODIFIED MODEL UA-751 DIGITAL SPHYGMONOMETER?

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 MODIFIED MODEL UA-751 DIGITAL SPHYGMONOMETER?

The FDA product code for MODIFIED MODEL UA-751 DIGITAL SPHYGMONOMETER is DXN.

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Related Devices (Code: DXN)

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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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