510(k) K862340 ยท IZW Collimator, Automatic, Radiographic
SENTEC LASER GUIDE LINE, MODEL SGL-05
| Applicant | Sentec Corp., Birmingham MI, US |
| Decision | Substantially Equivalent, Jul 11, 1986 |
| Received | Jun 20, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862340
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.