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FDA 510(k) Applications Submitted by TSK Laboratory International Japan KK
FDA 510(k) Number
Submission Date
Device Name
Applicant
K231734
06/14/2023
STERiJECT Low Dead Space, STERiJECT The Invisible Needle
TSK Laboratory International Japan KK
K242073
07/16/2024
STERiJECT Ophthalmic Needle; STERiJECT Ophthalmic Needle Low Dead Space (LDS)
TSK Laboratory International Japan KK
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