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PAGEWRITER CARDIOGRAPH

K080999 Class II Special
Decision Date
2008-05-09
Sponsor / Applicant
Philips Medical Systems

Technical Specification

510(k) Submission ID K080999
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 2008-05-09
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PAGEWRITER CARDIOGRAPH received FDA 510(k) clearance under submission number K080999, sponsored by Philips Medical Systems. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2008-05-09.

Classification & Regulation

This clearance is catalogued under FDA product code DPS and 21 CFR 870.2340, within the Cardiovascular review panel as a Class II device.