Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K023585
Device Classification Name
Set, Administration, Intravascular
More FDA Info for this Device
510(K) Number
K023585
Device Name
Set, Administration, Intravascular
Applicant
INTRAVASCULAR INCORPORATED
3600 BUR WOOD DR.
WAUKEGAN, IL 60085 US
Other 510(k) Applications for this Company
Contact
STEVE APERAVICH
Other 510(k) Applications for this Contact
Regulation Number
880.5440
More FDA Info for this Regulation Number
Classification Product Code
FPA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/25/2002
Decision Date
11/21/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact