FDA 510(k) Application Details - K992636

Device Classification Name	Display, Cathode-Ray Tube, Medical   More FDA Info for this Device
510(K) Number	K992636
Device Name	Display, Cathode-Ray Tube, Medical
Applicant	HEWLETT-PACKARD CO. 3000 MINUTEMAN RD. ANDOVER, MA 01810-1085 US Other 510(k) Applications for this Company
Contact	MIKE HUDON 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	08/06/1999
Decision Date	08/31/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review