| K-number | K821757 |
| Device name | QUIK - PREP2 ELECTRODE |
| Applicant | Quinton, Inc. |
| Product code | DRX |
| Device class | Class II |
| Decision date | Jul 2, 1982 |
| 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