| Record ID | K924110 |
|---|---|
| Device Name | LEOCOR CORFLO PUMP -- MODIFICATION |
| Applicant | Leocor, Inc. |
| Product Code | DQI · Cardiovascular |
| Decision Date | Sep 1, 1992 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 870.1800 |
| Device Class | Class 2 |
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