510(k) K823693 ยท FMI Needle, Hypodermic, Single Lumen
MYELOGRAPHY NEEDLE
| Applicant | Ocean Medical Products, Ltd., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 7, 1983 |
| Received | Dec 8, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823693
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.