Covidien · Class II · Cleared Sep 15, 2010
| K-number | K102291 |
| Device name | COVIDIEN ENDO GIA RADIAL RELOAD WITH TRI-STAPLE TECHNOLOGY |
| Applicant | Covidien |
| Product code | GDW |
| Device class | Class II |
| Decision date | Sep 15, 2010 |
| Decision | Substantially Equivalent |
| Regulation | 878.4750 |
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