Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by LEVO AG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K051387
05/27/2005
LEVO COMFORT II
LEVO AG
K140706
03/21/2014
LEVO MAX
LEVO AG
K083017
10/09/2008
LEVO C3
LEVO AG
K030893
03/21/2003
LEVO COMBI
LEVO AG
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact