510(k) K951132 ยท HLI Ophthalmoscope, Ac-Powered
ANGIOSCAN (AS STAND ALONE INSTRUMENT)
| Applicant | Carl Zeiss Meditec, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jun 26, 1995 |
| Received | Mar 13, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951132
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.