FDA issued a draft guidance Transfer of a Premarket Notification (510(k)) Clearance Questions and Answers” dated Dec. 22, 2014. This guidance explicitly states that when a device is sold or transferred to another party FDA does not expect submission of a new 510(k). Now that 510(k) numbers are included in Device listings and required to be updated information FDA will now use this information to indicate the current holder of the device 510(k) and can be updated by manufacturers as needed and if needed outside the annual filing no additional fee is required.
It also states: “Because contract manufacturers and sterilizers, foreign exporters, and foreign private label distributors are not responsible for the commercial distribution of devices, they would not be 510(k) holders, and should list the product under their customer?s 510(k) number once it has been listed by the 510(k) holder.”
If more than one entity claims the same 510(k) within the same annual update period the most recent update is used by the database. FDA will contact the parties to determine the rightful owner.