Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K032619
Device Classification Name
Device, Neurovascular Embolization
More FDA Info for this Device
510(K) Number
K032619
Device Name
Device, Neurovascular Embolization
Applicant
SURGICA CORP.
5090 ROBERT J. MATHEWS PKWY.
#4
EL DORADO HILLS, CA 95762 US
Other 510(k) Applications for this Company
Contact
LOU MATSON
Other 510(k) Applications for this Contact
Regulation Number
882.5950
More FDA Info for this Regulation Number
Classification Product Code
HCG
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/26/2003
Decision Date
02/13/2004
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact