510(k) K101861 ยท HKI Camera, Ophthalmic, Ac-Powered
TRUEVISION 3D VISUALIZATION AND GUIDANCE SYSTEM
| Applicant | Truevision Systems, Incorporated, Santa Barbara CA, US |
| Decision | Substantially Equivalent, Dec 22, 2010 |
| Received | Jul 2, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101861
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.