Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K090679
Device Classification Name
Device,Anastomotic,Microvascular
More FDA Info for this Device
510(K) Number
K090679
Device Name
Device,Anastomotic,Microvascular
Applicant
VIOPTIX, INC.
3722 AVE. SAUSALITO
IRVINE, CA 92606 US
Other 510(k) Applications for this Company
Contact
GRACE HOLLAND
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
MVR
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/16/2009
Decision Date
04/17/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact