FDA 510(k) Applications Submitted by Ranfac Corporation

FDA 510(k) Number Submission Date Device Name Applicant
K190177 02/01/2019 J-Type Marrow Biopsy Needle,T-Type Marrow Biopsy Needle,Tweezer Bone Marrow Biopsy Needle, Ranfac Corporation
K202287 08/12/2020 Ran-Flex-B Bone Marrow Aspiration Needle Ranfac Corporation
K183146 11/13/2018 Ranfac Cartilage Biopsy Needle Ranfac Corporation
K223612 12/05/2022 Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA) Ranfac Corporation


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