510(k) K910089 ยท FMJ Manometer, Spinal-Fluid
MEGA LUMBAR PUNCTURE KIT
| Applicant | Megadyne Medical Products, Inc., Tampa FL, US |
| Decision | Unknown, Jun 20, 1991 |
| Received | Jan 9, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910089
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.