510(k) K924401 ยท GGC Control, Plasma, Abnormal
PATHOPLASMA(R) I & II (PATH CITRATED HUMAN PLASMA)
| Applicant | Behring Diagnostics, Inc., Westwood MA, US |
| Decision | Substantially Equivalent, Feb 22, 1994 |
| Received | Aug 31, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924401
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.