FDA 510(k) Application Details - K151249

Device Classification Name	Container, Sharps   More FDA Info for this Device
510(K) Number	K151249
Device Name	Container, Sharps
Applicant	PUREWAY COMPLIANCE, INC 201 SANTA MONICA BLVD. SUITE 400 SANTA MONICA, CA 90401 US Other 510(k) Applications for this Company
Contact	JEFFERY MIGLICCO 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	05/12/2015
Decision Date	09/04/2015
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