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

FDA 510(k) Number Submission Date Device Name Applicant
K080060 01/09/2008 VIVOSONIC NEUROSCREEN VIVOSONIC, INC.
K043396 12/10/2004 INTEGRITY, MODEL V500 VIVOSONIC, INC.
K003364 10/27/2000 VIVO 200 DPS VIVOSCAN VIVOSONIC, INC.
K033108 09/30/2003 VIVO 200 DPS VIVOSCAN VERSION 2.0 OAE AUDIOMETER VIVOSONIC, INC.


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