510(k) K232991 ยท QGL Transcutaneous Nerve Stimulator For Adhd
BT-1000
| Applicant | Bistos Co., Ltd., Gyeonggi, KR |
| Decision | Substantially Equivalent, Aug 28, 2024 |
| Received | Sep 22, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232991
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.