Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Haemachem, Inc. — Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K903874 | FIBRINOTEST(TM) - FIBRINOGEN ASSAY | Haemachem, Inc. | 1991-02-14 | 176 | 0 |
| K853239 | HEPTEST-A QUANTITATIVE HEPARIN IN PLASMA ASSAY | Haemachem, Inc. | 1985-11-05 | 96 | 0 |
| K841956 | BOVINE THROMBIN, HUMAN THROMBIN | Haemachem, Inc. | 1984-07-19 | 66 | 0 |
| K841957 | BOVINE FACTOR XA-HUMAN FACTOR XA | Haemachem, Inc. | 1984-07-19 | 66 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda