510(k) K252735 ยท OWB Interventional Fluoroscopic X-Ray System
C-beam
| Applicant | Pulmera, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, May 22, 2026 |
| Received | Aug 28, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252735
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.