Hemagen Diagnostics, Inc. · Class II · Cleared Jul 16, 1993
| K-number | K932373 |
| Device name | HEMAGEN CARDIOLIPIN ANTIBODY KIT (EIA METHOD0 |
| Applicant | Hemagen Diagnostics, Inc. |
| Product code | MID |
| Device class | Class II |
| Decision date | Jul 16, 1993 |
| Decision | Substantially Equivalent |
| Regulation | — |
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