510(k) K230268 ยท GEX Powered Laser Surgical Instrument
ZenPro 40
| Applicant | BLUECORE COMPANY Co., Ltd., Busan, KR |
| Decision | Substantially Equivalent, Aug 10, 2023 |
| Received | Jan 31, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230268
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.