510(k) K883471 ยท HLP Target, Fusion And Stereoscopic
VKG 1000, VIDEO KERATOMETER
| Applicant | Technitex, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Nov 8, 1988 |
| Received | Aug 16, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883471
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.