meddevicedb.com FDA Device Reference

PageWriter TC20 Cardiograph, PageWriter TC30 Cardiograph, PageWriter TC50 Cardiograph, PageWriter TC70 Cardiograph

K191738 Class II Traditional
Decision Date
2020-09-29
Sponsor / Applicant
Philips Medical Systems

Technical Specification

510(k) Submission ID K191738
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 2020-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PageWriter TC20 Cardiograph, PageWriter TC30 Cardiograph, PageWriter TC50 Cardiograph, PageWriter TC70 Cardiograph received FDA 510(k) clearance under submission number K191738, 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 2020-09-29.

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.