510(k) DEN220006 ยท QSW Endoscopic Traction Device
ProdiGI
| Applicant | Covidien, LLC, Santa Clara CA, US |
| Decision | Unknown, Jun 13, 2022 |
| Received | Jan 14, 2022 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN220006
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.