FDA 510(k) Application Details - K980587

Device Classification Name	Set, I.V. Fluid Transfer   More FDA Info for this Device
510(K) Number	K980587
Device Name	Set, I.V. Fluid Transfer
Applicant	INRAD 3956 44TH ST., S.E. KENTWOOD, MI 49512 US Other 510(k) Applications for this Company
Contact	ANNE ARMSTRONG Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	LHI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/17/1998
Decision Date	04/17/1998
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