510(k) K930923 ยท GGC Control, Plasma, Abnormal
COAG-CONTROL
| Applicant | American Bioproducts Co., Parsippany NJ, US |
| Decision | Substantially Equivalent, Apr 27, 1993 |
| Received | Feb 23, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930923
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.