FDA 510(k) Application Details - K990866

Device Classification Name	Exerciser, Measuring   More FDA Info for this Device
510(K) Number	K990866
Device Name	Exerciser, Measuring
Applicant	QUINTON, INC. 3303 MONTE VILLA PKWY. BOTHELL, WA 98021-8906 US Other 510(k) Applications for this Company
Contact	MATTHEW J HEDLUND Other 510(k) Applications for this Contact
Regulation Number	890.5360   More FDA Info for this Regulation Number
Classification Product Code	ISD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/16/1999
Decision Date	04/29/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review