510(k) K911059 ยท LIE Reagent/Device, Inoculum Calibration
TURBIDOMETRIC STANDARD
| Applicant | Scientific Device Laboratory, Inc., Glenview IL, US |
| Decision | Substantially Equivalent, Jun 10, 1991 |
| Received | Mar 11, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911059
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.