510(k) K243764 ยท NVK Laser, Dental, Soft Tissue
Medical Diode Laser (UTU3-F7B,UTU3-F7W,UTU3-G7B,UTU3-G7W,UTU-G20B,UTU-G20W)
| Applicant | Wuhan Pioon Technology Co., Ltd., Wuhan, CN |
| Decision | Substantially Equivalent, May 8, 2025 |
| Received | Dec 6, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243764
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.