FDA 510(k) Application Details - K170813

Device Classification Name	X-Ray, Tomography, Computed, Dental   More FDA Info for this Device
510(K) Number	K170813
Device Name	X-Ray, Tomography, Computed, Dental
Applicant	PaloDEx Group Oy Nahkelantie 160 Tuusula 04300 FI Other 510(k) Applications for this Company
Contact	Terho Turkumaki Other 510(k) Applications for this Contact
Regulation Number	892.1750   More FDA Info for this Regulation Number
Classification Product Code	OAS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/17/2017
Decision Date	04/07/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review