Contour Medical Technology, Inc. · Class II · Cleared Mar 4, 1997
| K-number | K970125 |
| Device name | NOAH MONITORING ELECTRODE SYSTEM |
| Applicant | Contour Medical Technology, Inc. |
| Product code | DRX |
| Device class | Class II |
| Decision date | Mar 4, 1997 |
| 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