Valleylab, Inc. · Class II · Cleared Jan 25, 1989
| K-number | K885262 |
| Device name | POLYHESIVE MONITORING AND DIAGNOSTIC ELECTRODES |
| Applicant | Valleylab, Inc. |
| Product code | DRX |
| Device class | Class II |
| Decision date | Jan 25, 1989 |
| 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