RELIEF
Device Facts
| Record ID | K812567 |
|---|---|
| Device Name | RELIEF |
| Applicant | American Pharmaceutical Co., Inc. |
| Product Code | LKX · GU |
| Decision Date | Nov 10, 1981 |
| Decision | SESE |
| Submission Type | Traditional |
| Device Class | Class U |
| Record ID | K812567 |
|---|---|
| Device Name | RELIEF |
| Applicant | American Pharmaceutical Co., Inc. |
| Product Code | LKX · GU |
| Decision Date | Nov 10, 1981 |
| Decision | SESE |
| Submission Type | Traditional |
| Device Class | Class U |
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