FDA 510(k) Applications Submitted by CT INTL.

FDA 510(k) Number Submission Date Device Name Applicant
K981304 04/10/1998 NITRILON CORRECT-TOUCH CT INTL.
K984512 12/18/1998 NITRILON CORRECT-TOUCH CT INTL.


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