FDA 510(k) Application Details - K001337

Device Classification Name	Container, Sharps   More FDA Info for this Device
510(K) Number	K001337
Device Name	Container, Sharps
Applicant	THE DANIELS CORP. 4329 GRAYDON RD. SAN DIEGO, CA 92130 US Other 510(k) Applications for this Company
Contact	FLOYD G LARSON 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	04/27/2000
Decision Date	07/05/2000
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