| Record ID | K833421 |
|---|---|
| Device Name | PROGRAMMABLE STIMULATOR 2352 |
| Applicant | Medtronic Vascular |
| Product Code | JOQ · Cardiovascular |
| Decision Date | Jan 30, 1984 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 870.1750 |
| Device Class | Class 2 |
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