510(k) K923771 ยท DHR System, Test, Rheumatoid Factor
PULSE RF TEST
| Applicant | Pulse Scientific, Inc., Burlington, Ont., Canada, CA |
| Decision | Substantially Equivalent, Oct 5, 1992 |
| Received | Jul 28, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923771
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.