FDA 510(k) Application Details - K972365

Device Classification Name	System, X-Ray, Mobile   More FDA Info for this Device
510(K) Number	K972365
Device Name	System, X-Ray, Mobile
Applicant	EUROTEC, S.R.L. 5/7, VIA ALDO MORO SCANZOROSCIATE (BG) 24020 IT Other 510(k) Applications for this Company
Contact	CHRISTIAN BONAZZI Other 510(k) Applications for this Contact
Regulation Number	892.1720   More FDA Info for this Regulation Number
Classification Product Code	IZL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/25/1997
Decision Date	12/12/1997
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