FDA 510(k) Applications Submitted by THEYFIT

FDA 510(k) Number Submission Date Device Name Applicant
K150072 01/14/2015 TheyFit Male Condom THEYFIT
K122219 07/25/2012 THEYFIT MALE CONDOM THEYFIT


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