510(k) K952521 ยท MID System, Test, Anticardiolipin Immunological
CARDIOLIPIN IGM EIA TEST SYSTEM
| Applicant | Immunoprobe, Inc., Washington, D.C. DC, US |
| Decision | Substantially Equivalent, Feb 9, 1996 |
| Received | Jun 1, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952521
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.