FDA 510(k) Applications Submitted by IMDS Operations B.V.

FDA 510(k) Number Submission Date Device Name Applicant
K200324 02/10/2020 NHancer Rx IMDS Operations B.V.
K121077 04/09/2012 NHANCER IMDS OPERATIONS B.V.
K210110 01/19/2021 Guidion IMDS Operations B.V.
K210431 02/12/2021 ReCross IMDS Operations B.V.
K191229 05/08/2019 TrapIt IMDS Operations B.V.
K223728 12/13/2022 Micro Rx IMDS Operations B.V.


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