Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K143652
Device Classification Name
Catheter, Angioplasty, Peripheral, Transluminal
More FDA Info for this Device
510(K) Number
K143652
Device Name
Catheter, Angioplasty, Peripheral, Transluminal
Applicant
Vector Corporation LLC
1270 Ave of Americas, Suite 302
New York, NY 10020 US
Other 510(k) Applications for this Company
Contact
Jay Sturm
Other 510(k) Applications for this Contact
Regulation Number
870.1250
More FDA Info for this Regulation Number
Classification Product Code
LIT
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/23/2014
Decision Date
02/26/2015
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact