510(k) K180689 ยท PKL Hemostatic Metal Clip For The Gi Tract
Padlock Clip defect closure device; Padlock Clip Pro-Select defect closure device
| Applicant | STERIS Corporation, Mentor OH, US |
| Decision | Substantially Equivalent, Apr 12, 2018 |
| Received | Mar 15, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K180689
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.