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

FDA 510(k) Number Submission Date Device Name Applicant
K130538 03/01/2013 WINX SLEEP THERAPY SYSTEM APNICURE, INC.
K111549 06/03/2011 ATTUNE SLEEP APNEA SYSTEM APNICURE, INC.
K132003 07/01/2013 WINX SLEEP THERAPY SYSTEM APNICURE, INC.
K122130 07/18/2012 WINX SLEEP THERAPY SYSTEM APNICURE, INC.


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