510(k) K880477 ยท GMQ Antigens, Nontreponemal, All
RPR TEST FOR SYPHILIS IN SERUM OR PLASMA
| Applicant | Ampcor, Inc., Bridgeport NJ, US |
| Decision | Substantially Equivalent, Mar 30, 1988 |
| Received | Feb 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880477
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.