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

FDA 510(k) Number Submission Date Device Name Applicant
K120563 02/24/2012 KEYPATH MRSA/MSSA BLOOD CULTURE TEST-BT MICROPHAGE, INC.
K102342 08/18/2010 KEYPATH(TM) MRSA/MSSA BLOOD CULTURE TEST- BT MICROPHAGE, INC.


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