FDA 510(k) Application Details - K113842

Device Classification Name	More FDA Info for this Device
510(K) Number	K113842
Device Name	CATHETER CONNECTIONS' DUALCAP SOLO
Applicant	CATHETER CONNECTIONS, INC. 2455 E Parleys Way - Suite 150 Salt Lake City, UT 84109 US Other 510(k) Applications for this Company
Contact	DONALD D SOLOMON Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QBP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/28/2011
Decision Date	01/27/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review