Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K091214
Device Classification Name
Catheter, Umbilical Artery
More FDA Info for this Device
510(K) Number
K091214
Device Name
Catheter, Umbilical Artery
Applicant
FOOTPRINT MEDICAL
1203 CAMDEN ST.
SAN ANTONIO, TX 78215 US
Other 510(k) Applications for this Company
Contact
CLYDE BAKER
Other 510(k) Applications for this Contact
Regulation Number
880.5200
More FDA Info for this Regulation Number
Classification Product Code
FOS
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/27/2009
Decision Date
09/25/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact