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MODIFIED MODEL UA-751 DIGITAL SPHYGMONOMETER

K871719 Class II Traditional
Decision Date
1987-06-05
Sponsor / Applicant
A&D Engineering, Inc.

Technical Specification

510(k) Submission ID K871719
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 1987-06-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFIED MODEL UA-751 DIGITAL SPHYGMONOMETER received FDA 510(k) clearance under submission number K871719, sponsored by A&D Engineering, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1987-06-05.

Classification & Regulation

This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.