FDA 510(k) Application Details - K051402

Device Classification Name	Camera, Scintillation (Gamma)   More FDA Info for this Device
510(K) Number	K051402
Device Name	Camera, Scintillation (Gamma)
Applicant	GVI TECHNOLOGY PARTNERS 1470 ENTERPRISE PKWY. TWINSBURG, OH 44087 US Other 510(k) Applications for this Company
Contact	KEVIN M MURROCK Other 510(k) Applications for this Contact
Regulation Number	892.1100   More FDA Info for this Regulation Number
Classification Product Code	IYX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/31/2005
Decision Date	06/13/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review