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A-PLUS ARTERIAL PULSE WAVEFORM ANALYSIS SYSTEM AND PC SOFTWARE

K072593 Class II Traditional
Decision Date
2007-11-15
Sponsor / Applicant
Healthstats International Pte. , Ltd.

Technical Specification

510(k) Submission ID K072593
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2007-11-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

A-PLUS ARTERIAL PULSE WAVEFORM ANALYSIS SYSTEM AND PC SOFTWARE received FDA 510(k) clearance under submission number K072593, sponsored by Healthstats International Pte. , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2007-11-15.

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.