510(k) K904753 ยท IWE Monitor, Patient Position, Light-Beam
DIOLASE
| Applicant | Scanditronix, Inc., Sweden, SE |
| Decision | Substantially Equivalent, Nov 9, 1990 |
| Received | Oct 19, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904753
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.