510(k) K832031 ยท KTL Anti-Dna Indirect Immunofluorescent Solid Phase
ANTI-N DNA ANTIBODY TEST KIT
| Applicant | Breit Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 11, 1983 |
| Received | Jun 23, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832031
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.