510(k) K072920 ยท GJS Test, Time, Prothrombin
HANDHELD BASE UNIT
| Applicant | Roche Diagnostics Corp., Indianapolis IN, US |
| Decision | Substantially Equivalent, Jan 31, 2008 |
| Received | Oct 15, 2007 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K072920
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.