Cape Tech Medical Products · Class II · Cleared Aug 5, 1993
| K-number | K926039 |
| Device name | GUIDE-TECH ENCAPSULATED GUIDEWIRE |
| Applicant | Cape Tech Medical Products |
| Product code | KNY |
| Device class | Class II |
| Decision date | Aug 5, 1993 |
| Decision | Substantially Equivalent |
| Regulation | 876.5130 |
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