510(k) K183485 ยท LDK Device, Sensing, Optical Contour
CryoVizion System
| Applicant | Cryos Technologies, Inc., Joliette, CA |
| Decision | Substantially Equivalent, Aug 28, 2019 |
| Received | Dec 17, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183485
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.