Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
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
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact