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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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