FDA 510(k) Application Details - K132476

Device Classification Name	Container, Sharps   More FDA Info for this Device
510(K) Number	K132476
Device Name	Container, Sharps
Applicant	GRP & ASSOCIATES 816 CONGRESS, SUITE 1400 AUSTIN, TX 78701 US Other 510(k) Applications for this Company
Contact	ROBERT SEIPLE Other 510(k) Applications for this Contact
Regulation Number	880.5570   More FDA Info for this Regulation Number
Classification Product Code	MMK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/08/2013
Decision Date	05/02/2014
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