FDA 510(k) Application Details - K973459

Device Classification Name	Densitometer, Bone   More FDA Info for this Device
510(K) Number	K973459
Device Name	Densitometer, Bone
Applicant	NORLAND CORP. WEST 6340 HACKBARTH RD. FORT ATKINSON, WI 53538-8999 US Other 510(k) Applications for this Company
Contact	TERRY SCHWALENBERG Other 510(k) Applications for this Contact
Regulation Number	892.1170   More FDA Info for this Regulation Number
Classification Product Code	KGI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/12/1997
Decision Date	02/13/1998
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