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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.
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