510(k) K872360 ยท GHH Fibrin Split Products
DATA-FI FIBRIN(OGEN) DEGRADATION PROD.(FDP)DET SET
| Applicant | American Dade, Santa Ana CA, US |
| Decision | Substantially Equivalent, Jul 6, 1987 |
| Received | Jun 18, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872360
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 22, 2005 | Dade Behring , Inc. Dade Fibrin(ogen) Degradation Products (FDP) Detection Set. Catalog number B4233-10E Terminated |
GHH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.