Covidien, Formerly US Surgical A Divison of Tyco H · Class II · Cleared Jul 1, 2013
| K-number | K131705 |
| Device name | ENDO GIA RADIAL RELOAD WITH TRI-STAPLE TECHNOLOGY |
| Applicant | Covidien, Formerly US Surgical A Divison of Tyco H |
| Product code | GDW |
| Device class | Class II |
| Decision date | Jul 1, 2013 |
| 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