FDA 510(k) Applications Submitted by AMS Diagnostics
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K172232 | 07/25/2017 | LIASYS 600 Electrolyte Measurement System, LIASYS 600 Creatinine reagent, LIASYS 600 | AMS Diagnostics |
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