FDA 510(k) Applications Submitted by BOEHRINGER LABORATORIES LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K151990 | 07/20/2015 | Tissue Removal System | BOEHRINGER LABORATORIES LLC |
| K234033 | 12/20/2023 | ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340) | Boehringer Laboratories LLC |
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