FDA 510(k) Application Details - K942530

Device Classification Name	Sleeve, Limb, Compressible   More FDA Info for this Device
510(K) Number	K942530
Device Name	Sleeve, Limb, Compressible
Applicant	ACI MEDICAL, INC. 1857 DIAMOND ST. SAN MARCOS, CA 92069 US Other 510(k) Applications for this Company
Contact	ED ARKANS 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	05/27/1994
Decision Date	02/28/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review