510(k) K991302 ยท IXC Illuminator, Radiographic-Film
SMARTLIGHT DIGITAL FILM VIEWER, MODELS SL 4000PLUS, SL 2000PLUS
| Applicant | Smartlight, Inc., Hackensack NJ, US |
| Decision | Substantially Equivalent, Jun 1, 1999 |
| Received | Apr 16, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991302
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.