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ELECTRONIC BLOOD PRESSURE MONITOR FOR UPPER ARM

K130232 Class II Abbreviated
Decision Date
2013-09-17
Sponsor / Applicant
Jinxinbao Electronic Co.,Ltd

Technical Specification

510(k) Submission ID K130232
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2013-09-17
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRONIC BLOOD PRESSURE MONITOR FOR UPPER ARM received FDA 510(k) clearance under submission number K130232, sponsored by Jinxinbao Electronic Co.,Ltd. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2013-09-17.

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.