510(k) K823255 ยท FMI Needle, Hypodermic, Single Lumen
NON-STERILE REUSABLE NEEDLES
| Applicant | Vertex Medical Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 22, 1982 |
| Received | Nov 1, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823255
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.