510(k) K212774 ยท LRC Instrument, Ent Manual Surgical
VenSure LightGuide
| Applicant | Intersect Ent., Menlo Park CA, US |
| Decision | Substantially Equivalent, Feb 4, 2022 |
| Received | Sep 1, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212774
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.