510(k) K941904 ยท JRE Refractometer For Clinical Use
MODEL A300CL CLINICAL REFRACTOMETER
| Applicant | Vee Gee Scientific, Inc., Kirkland WA, US |
| Decision | Substantially Equivalent, Dec 13, 1994 |
| Received | Apr 19, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941904
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.