510(k) K810640 ยท KQX Goniometer, Ac-Powered
POLARISED LIGHT GRONIOMETER
| Applicant | Cairco , Ltd., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 17, 1981 |
| Received | Mar 10, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810640
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.