Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by VORTEK SURGICAL, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K080341
02/08/2008
ENDODRAPE(TM)
VORTEK SURGICAL, LLC
K070406
02/12/2007
ENDODRAPE
VORTEK SURGICAL, LLC
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact