510(k) K880164 ยท DHR System, Test, Rheumatoid Factor
RF CARD TEST & RF LIQUID TEST
| Applicant | Ampcor, Inc., Bridgeport NJ, US |
| Decision | Substantially Equivalent, Feb 10, 1988 |
| Received | Jan 13, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880164
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.