FDA 510(k) Application Details - K123289

Device Classification Name	Wrap, Sterilization   More FDA Info for this Device
510(K) Number	K123289
Device Name	Wrap, Sterilization
Applicant	CARDINAL HEALTH-MEDICAL PRODUCTS AND SERVICES 1430 WAUKEGAN RD. MCGAW PARK, IL 60085 US Other 510(k) Applications for this Company
Contact	LAVENIA FORD Other 510(k) Applications for this Contact
Regulation Number	880.6850   More FDA Info for this Regulation Number
Classification Product Code	FRG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/22/2012
Decision Date	02/28/2013
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	Y
Expedited Review