Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by Livetec GMBH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K131797
06/18/2013
3B LASER NEEDLE
LIVETEC GMBH
K142215
08/12/2014
Power Twin21-50/Power Twin21-100
LIVETEC GMBH
K142722
09/23/2014
3B Laser 500, 3B Laser 200, LA-X P 500, LA-X P 200
Livetec GMBH
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact