FDA 510(k) Applications Submitted by ARCOMA AB
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K073632 | 12/26/2007 | INTUITION, MODEL 0170 | ARCOMA AB |
| K140683 | 03/18/2014 | 0180 INTUITION, 0072 PRECISION | ARCOMA AB |
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