510(k) K000229 ยท FCW Light Source, Fiberoptic, Routine
VIDEOLABS MEDCAM PROPLUS VIDEO CAMERA AND INTEGRAL LIGHT SOURCE
| Applicant | Videolabs, Inc., Saint Louis Park MN, US |
| Decision | Substantially Equivalent, Mar 21, 2000 |
| Received | Jan 27, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000229
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.