510(k) K913314 ยท HKI Camera, Ophthalmic, Ac-Powered
CANDELA RETINAL CAMERA
| Applicant | Candela Laser Corp., Wayland MA, US |
| Decision | Substantially Equivalent, Jan 23, 1992 |
| Received | Jul 25, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913314
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.