| K-number | K170524 |
| Device name | Access AMH |
| Applicant | Beckman Coulter, Inc. |
| Product code | PQO |
| Device class | Class II |
| Decision date | Nov 13, 2017 |
| Decision | Substantially Equivalent |
| Regulation | 862.1092 |
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View the full FDA submission: accessdata.fda.gov