FDA 510(k) Application Details - K011176

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K011176
Device Name	Syringe, Piston
Applicant	LOCKETT MEDICAL CORP. THREE RICHMOND SQUARE PROVIDENCE, RI 02906 US Other 510(k) Applications for this Company
Contact	WILLIAM LOCKETT III Other 510(k) Applications for this Contact
Regulation Number	880.5860   More FDA Info for this Regulation Number
Classification Product Code	FMF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/17/2001
Decision Date	08/10/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review