FDA 510(k) Application Details - K982203

Device Classification Name	System, X-Ray, Angiographic   More FDA Info for this Device
510(K) Number	K982203
Device Name	System, X-Ray, Angiographic
Applicant	PIE MEDICAL EQUIPMENT B.V. PHILIPSWEG 1 MAASTRICHT 6227 AJ NL Other 510(k) Applications for this Company
Contact	FRANK ANIBA Other 510(k) Applications for this Contact
Regulation Number	892.1600   More FDA Info for this Regulation Number
Classification Product Code	IZI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/22/1998
Decision Date	07/14/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review