FDA 510(k) Application Details - K080779

Device Classification Name	Lavage, Jet   More FDA Info for this Device
510(K) Number	K080779
Device Name	Lavage, Jet
Applicant	IRRIMAX CORPORATION 111 LAUREL RIDGE DRIVE ALPHARETTA, GA 30004 US Other 510(k) Applications for this Company
Contact	JULIE STEPHENS Other 510(k) Applications for this Contact
Regulation Number	880.5475   More FDA Info for this Regulation Number
Classification Product Code	FQH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/19/2008
Decision Date	02/04/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review