Terumo Medical Corp. · Class II · Cleared Apr 29, 1993
| K-number | K926214 |
| Device name | GUIDE WIRE FOR LAPOROSCOPIC USE |
| Applicant | Terumo Medical Corp. |
| Product code | GCJ |
| Device class | Class II |
| Decision date | Apr 29, 1993 |
| Decision | Substantially Equivalent |
| Regulation | 876.1500 |
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