Medtronic, Inc. · Class II · Cleared Oct 22, 2013
| K-number | K132673 |
| Device name | 5F & 6F LAUNCHER GUIDE CATHETER, 5F SHERPA ACTIVE NX GUIDE CATHETER, 6F Z4 GUIDING CATHETER |
| Applicant | Medtronic, Inc. |
| Product code | DQY |
| Device class | Class II |
| Decision date | Oct 22, 2013 |
| Decision | Substantially Equivalent |
| Regulation | 870.1250 |
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