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

FDA 510(k) Number Submission Date Device Name Applicant
K040484 02/25/2004 MAXO2+, MODEL A AND AE MAXTEC, INC.
K063488 11/17/2006 MAXO2 CU MAXTEC, INC.
K133540 11/18/2013 FLOCAP MAXTEC, INC.
K113232 11/02/2011 MAXMIXING BLOCK MAXTEC, INC.


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