FDA 510(k) Applications Submitted by ELTECH, S.R.L.

FDA 510(k) Number Submission Date Device Name Applicant
K050070 01/12/2005 K-LASER, MODELS 3,4,4D,6D ELTECH, S.R.L.
K091497 05/20/2009 K-LASER K-1200, MODEL 12 W ELTECH, S.R.L.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact