510(k) K213824 ยท LFL Instrument, Ultrasonic Surgical
Sonopet iQ Ultrasonic Aspirator System
| Applicant | Stryker Corporation, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Feb 3, 2022 |
| Received | Dec 8, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K213824
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.