510(k) K974240 ยท IZX Collimator, Manual, Radiographic
LIGHTLINE-M
| Applicant | Wuestec Medical, Inc., Mobile AL, US |
| Decision | Substantially Equivalent, Dec 22, 1997 |
| Received | Nov 12, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974240
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.