510(k) K253121 ยท MQE Needle, Assisted Reproduction
Giftlife Single Lumen Oocyte Retrieval Needle, Giftlife Double Lumen Oocyte Retrieval Needle
| Applicant | Gimbo Medical Technology Shenzhen Co., Ltd., Shezhen, CN |
| Decision | Substantially Equivalent, Jun 15, 2026 |
| Received | Sep 25, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253121
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.