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FDA 510(k)

MODIFIED MODEL UA-731 DIGITAL SPHYGMOMANOMETER

K-Number: K871720 · 1987-07-29

ApplicantA&D Engineering, Inc.
Decision Date1987-07-29
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED MODEL UA-731 DIGITAL SPHYGMOMANOMETER 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 1987-07-29 under 510(k) number K871720. 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 MODIFIED MODEL UA-731 DIGITAL SPHYGMOMANOMETER?

MODIFIED MODEL UA-731 DIGITAL SPHYGMOMANOMETER is a medical device that received FDA 510(k) clearance on 1987-07-29. The listed applicant is A&D Engineering, Inc.. The 510(k) number is K871720.

When did MODIFIED MODEL UA-731 DIGITAL SPHYGMOMANOMETER receive FDA 510(k) clearance?

MODIFIED MODEL UA-731 DIGITAL SPHYGMOMANOMETER received FDA 510(k) clearance on 1987-07-29, under 510(k) number K871720.

Who is the listed applicant for MODIFIED MODEL UA-731 DIGITAL SPHYGMOMANOMETER?

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-731 DIGITAL SPHYGMOMANOMETER?

The FDA product code for MODIFIED MODEL UA-731 DIGITAL SPHYGMOMANOMETER is DSK.

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Other records listing A&D Engineering, Inc. as applicant

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Related Devices (Code: DSK)

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.

K231586Endophys Blood Pressure Monitor model BPM-30Endophys Technologies, LLCK160945Endophys Blood Pressure MonitorEndophys Holdings, LLCK080670MODIFICATION TO SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor MedicalK070795SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor Medical Pty, Ltd.K033738MONITORING SYSTEM, MODEL ARGUS PB-2200Schiller AGK021517ABP FOR WINDOWSRozinn Electronics, Inc.

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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