FDA 510(k) Applications Submitted by MICHAEL SWITZER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K111534 | 06/02/2011 | ABACUS 3CP | DIATRON US INC |
| K112755 | 09/21/2011 | ABACUS 5 | DIATRON US INC |
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