FDA 510(k) Application Details - K031662

Device Classification Name	Transducer, Pressure, Catheter Tip   More FDA Info for this Device
510(K) Number	K031662
Device Name	Transducer, Pressure, Catheter Tip
Applicant	RADI MEDICAL SYSTEMS AB PALMBLADSGATAN 10 UPPSALA S-754 50 SE Other 510(k) Applications for this Company
Contact	MATS GRANLUND Other 510(k) Applications for this Contact
Regulation Number	870.2870   More FDA Info for this Regulation Number
Classification Product Code	DXO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/28/2003
Decision Date	06/06/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review