510(k) K132475 ยท OWN Confocal Optical Imaging
FLUOBEAM 800 CLINIC LASER IMAGING DEVICE AND FLUOCASE 800 CONTROL SYSTEM
| Applicant | Fluoptics, Orinda CA, US |
| Decision | Substantially Equivalent, May 7, 2014 |
| Received | Aug 7, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132475
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.