510(k) K252893 · SDO Transcutaneous Electrical Spine Stimulator To Improve Skeletal Muscle Strength And Sensation
ExaStim® Stimulation System (EXA-001); ExaStim® Stimulation System (EXA-011); ReCure® Electrode Pad (PAD-003); ReCure® Electrode Pad (PAD-013)
| Applicant | Aneuvo, Los Angeles CA, US |
| Decision | Substantially Equivalent, Mar 27, 2026 |
| Received | Sep 11, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252893
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.