510(k) K191291 ยท MQE Needle, Assisted Reproduction
Wallace Dual Lumen Oocyte Recovery System
| Applicant | CooperSurgical, Inc., Trumbull CT, US |
| Decision | Substantially Equivalent, Jun 12, 2019 |
| Received | May 14, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K191291
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.