510(k) K172244 ยท KTL Anti-Dna Indirect Immunofluorescent Solid Phase
EUROIMMUN IFA: Crithidia luciliae (anti-dsDNA) EUROPattern
| Applicant | Euroimmun Us, Inc., Mountain Lakes NJ, US |
| Decision | Substantially Equivalent, Apr 20, 2018 |
| Received | Jul 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172244
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.