FDA 510(k) Applications for Medical Device Product Code "QYM"

FDA 510(k) Number Applicant Device Name Decision Date
K230951 Terumo Europe N.V. Terumo Injection Filter Needle (NF-3013RBKE05M) 10/18/2023
K242073 TSK Laboratory International Japan KK STERiJECT Ophthalmic Needle; STERiJECT Ophthalmic Needle Low Dead Space (LDS) 10/23/2024


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