510(k) K832142 ยท HPT Perimeter, Automatic, Ac-Powered
DICON GLAUCOMA DIAG. CENTER 2000 SERIES
| Applicant | CooperVision, Inc., Southampton, GB |
| Decision | Substantially Equivalent, Aug 1, 1983 |
| Received | Jul 5, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832142
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.