FDA 510(k) Applications Submitted by FUJI SYSTEMS CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K120781 | 03/15/2012 | CELLO BALLOON GUIDE CATHETER (6F), 950 MM AND 1020 MM LENGTH | FUJI SYSTEMS CORP. |
| K051522 | 06/08/2005 | SILBRONCHO DOUBLE LUMEN TUBE | FUJI SYSTEMS CORP. |
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