FDA 510(k) Application Details - K180534

Device Classification Name	Display, Cathode-Ray Tube, Medical   More FDA Info for this Device
510(K) Number	K180534
Device Name	Display, Cathode-Ray Tube, Medical
Applicant	Philips Medizin Systeme Boeblingen GmbH Hewlett-Packard Str. 2 Boeblingen 71034 DE Other 510(k) Applications for this Company
Contact	Michael Asmalsky Other 510(k) Applications for this Contact
Regulation Number	870.2450   More FDA Info for this Regulation Number
Classification Product Code	DXJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/28/2018
Decision Date	07/16/2018
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review