FDA 510(k) Application Details - K992079

Device Classification Name	Sleeve, Limb, Compressible   More FDA Info for this Device
510(K) Number	K992079
Device Name	Sleeve, Limb, Compressible
Applicant	THE KENDALL COMPANY, L.P. 15 HAMPSHIRE ST. MANSFIELD, MA 02048 US Other 510(k) Applications for this Company
Contact	PAUL W EVANS Other 510(k) Applications for this Contact
Regulation Number	870.5800   More FDA Info for this Regulation Number
Classification Product Code	JOW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/21/1999
Decision Date	09/29/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review