FDA 510(k) Applications Submitted by DIOMED, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K013499 10/22/2001 DIOMED 15 PLUS AND DIOMED 30PLUS LASERS DIOMED, INC.
K990014 01/04/1999 DIOSCAN DIOMED, INC.
K000982 03/27/2000 A100 AESTHETIC DIODE LASER DIOMED, INC.
K041957 07/21/2004 EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS DIOMED, INC.
K023543 10/22/2002 EVLT KIT AND D15PLUS AND D30PLUS DIODE DIOMED, INC.


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