510(k) K220891 ยท QUQ Knife, Intraocular Pressure Lowering
Kahook Dual Blade Glide (KDB Glide)
| Applicant | New World Medical, Inc., Rancho Cucamonga CA, US |
| Decision | Substantially Equivalent, May 17, 2024 |
| Received | Mar 28, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220891
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.