510(k) K991273 ยท MQE Needle, Assisted Reproduction
SWEMED FOLLICLE ASPIRATION SET, DOUBLE LUMEN, SINGLE LUMEN, AND LUER NEEDLE
| Applicant | Swemed Lab International AB, Washington DC, US |
| Decision | Substantially Equivalent, Aug 18, 1999 |
| Received | Apr 13, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991273
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.