FDA 510(k) Applications Submitted by Fujifilm Healthcare Americas Corporation
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K232314 | 08/02/2023 | Hood (DH-106STL, DH-116STL, DH-126STL, DH-096ST) | Fujifilm Healthcare Americas Corporation |
| K230752 | 03/17/2023 | Over-tube (TR-1208A); Over-tube (TR-1504A); Over-tube (TR-1507A) | Fujifilm Healthcare Americas Corporation |
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