FDA 510(k) Application Details - K992385

Device Classification Name	System,X-Ray,Extraoral Source,Digital   More FDA Info for this Device
510(K) Number	K992385
Device Name	System,X-Ray,Extraoral Source,Digital
Applicant	INSTRUMENTARIUM CORP. 300 WEST EDGERTON AVE. MILWAUKEE, WI 53207 US Other 510(k) Applications for this Company
Contact	TOMMI JOKINIEMI Other 510(k) Applications for this Contact
Regulation Number	872.1800   More FDA Info for this Regulation Number
Classification Product Code	MUH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/16/1999
Decision Date	09/28/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review