Cordis Corp. · Class II · Cleared Dec 15, 1982
| K-number | K823530 |
| Device name | STIMUCORD EXTERNAL NEURAL STIM. 911A |
| Applicant | Cordis Corp. |
| Product code | GZB |
| Device class | Class II |
| Decision date | Dec 15, 1982 |
| Decision | Substantially Equivalent |
| Regulation | 882.5880 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov