FDA 510(k) Applications Submitted by Marijn Van Stralen

FDA 510(k) Number Submission Date Device Name Applicant
K230197 01/25/2023 BoneMRI v1.6 MRIguidance B.V.
K221762 06/17/2022 BoneMRI v1.4 MRlguidance B.V.


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