510(k) K940386 ยท IXL Device, Spot-Film
KODAK AUTOMIXER III INTEGRATED, KODAK AUTOMIXER III 180 LP
| Applicant | Eastman Kodak Company, Rochester NY, US |
| Decision | Substantially Equivalent, Aug 17, 1994 |
| Received | Jan 26, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940386
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.