FDA 510(k) Application Details - K022340

Device Classification Name	Sleeve, Limb, Compressible   More FDA Info for this Device
510(K) Number	K022340
Device Name	Sleeve, Limb, Compressible
Applicant	DYNAMIC AIR, INC. 3495 BANKHEAD HIGHWAY SUITE A ATLANTA, GA 30331 US Other 510(k) Applications for this Company
Contact	BRENT KNIGHT 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	07/18/2002
Decision Date	02/19/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review