Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by COVIDEN (FORMERLY REGISTERED AS US SURGICAL, A DIV
FDA 510(k) Number
Submission Date
Device Name
Applicant
K103253
11/03/2010
SILS PORT
COVIDEN (FORMERLY REGISTERED AS US SURGICAL, A DIV
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact