510(k) K092229 ยท JZO System, Test, Thyroid Autoantibody
THYRETAIN TM TSI REPORTER BIOASSAY
| Applicant | Diagnostic Hybrids, Inc., Athens OH, US |
| Decision | Substantially Equivalent, May 18, 2010 |
| Received | Jul 23, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092229
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.