Midwest Monitoring · Class II · Cleared Mar 11, 1981
| K-number | K803179 |
| Device name | DISPOSABLE ELECTRODE FOR EKG |
| Applicant | Midwest Monitoring |
| Product code | DRX |
| Device class | Class II |
| Decision date | Mar 11, 1981 |
| Decision | Substantially Equivalent |
| Regulation | 870.2360 |
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