510(k) K260122 ยท QRL Multiple Use Blood Lancet For Single Patient Use Only
Lancing Device (PressGo, LDE3, LDE3AST, LDE5, EasyStep)
| Applicant | SteriLance Medical (Suzhou), Inc., Suzhou, CN |
| Decision | Substantially Equivalent, Jul 6, 2026 |
| Received | Jan 15, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260122
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.