FDA 510(k) Applications Submitted by NORLAND CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K980125	01/14/1998	REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER	NORLAND CORP.
K973104	08/19/1997	NORLAND MODEL PDEXA BONE DENSITOMETER	NORLAND CORP.
K980289	01/26/1998	FRACTURE RISK ASSESSMENT FOR THE NORLAND SXA 3000 BONE DENSITOMETER	NORLAND CORP.
K980569	02/13/1998	FRACTURE RISK ASSESSMENT CAPABILITY FOR NORLAND X-RAY BONE DENSITOMETERS	NORLAND CORP.
K973459	09/12/1997	NORLAND BODY COMPOSITION OPTION FOR NORLAND DEXA BONE DENSITOMETERS	NORLAND CORP.
K972882	08/05/1997	APOLLO	NORLAND CORP.