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CARECOMPANION PATIENT STATION/CARECOMPANION PATIENT STATION

K023286 Class II Traditional
Decision Date
2003-05-02
Sponsor / Applicant
Neptec Design Group, Ltd.

Technical Specification

510(k) Submission ID K023286
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2003-05-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CARECOMPANION PATIENT STATION/CARECOMPANION PATIENT STATION received FDA 510(k) clearance under submission number K023286, sponsored by Neptec Design Group, 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 2003-05-02.

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.