510(k) K944226 ยท DOX Fluorometer, Lead (Dedicated Instruments)
MSI PROCEDURE KIT
| Applicant | Msi, Inc., Tarpon Springs FL, US |
| Decision | Substantially Equivalent, Jun 21, 1995 |
| Received | Aug 30, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944226
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.