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PAGEWRITER TC 20, 30, 50, 70

K113144 Class II Traditional
Decision Date
2012-04-03
Sponsor / Applicant
Philips Medical Systems

Technical Specification

510(k) Submission ID K113144
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 2012-04-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PAGEWRITER TC 20, 30, 50, 70 received FDA 510(k) clearance under submission number K113144, sponsored by Philips Medical Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-04-03.

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.