Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K082034
Device Classification Name
Catheter, Thrombus Retriever
More FDA Info for this Device
510(K) Number
K082034
Device Name
Catheter, Thrombus Retriever
Applicant
CONCENTRIC MEDICAL, INC.
301 E. EVELYN AVE.
MOUNTAIN VIEW, CA 94041 US
Other 510(k) Applications for this Company
Contact
LARAINE PANGELINA
Other 510(k) Applications for this Contact
Regulation Number
870.1250
More FDA Info for this Regulation Number
Classification Product Code
NRY
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/17/2008
Decision Date
08/15/2008
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
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