FDA 510(k) Applications Submitted by VITAID, LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K050803 03/30/2005 PEDIATRIC CUFFED AND UNCUFFED ET TUBES; STANDARD CUFFED AND UNCUFFED ET TUBES VITAID, LTD.


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