FDA 510(k) Applications Submitted by ASHITAKA FACTORY OF TERUMO CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K170223 | 01/25/2017 | Progreat | ASHITAKA FACTORY OF TERUMO CORPORATION |
| K161546 | 06/03/2016 | R2P SlenGuide | ASHITAKA FACTORY OF TERUMO CORPORATION |
| K203521 | 12/01/2020 | FineCross M3 | Ashitaka Factory of Terumo Corporation |
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