Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
KPB — Predicate Candidate Screening
4 FDA 510(k) clearances under this product code; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K781875 | STAIN KIT FOR CELL CULTURES (30-100-00) | Flow Laboratories, Inc. | 1978-12-20 | 47 | 0 |
| K781874 | MYCOPLASMA ARGININI FITC (30-403-41) | Flow Laboratories, Inc. | 1978-12-20 | 47 | 0 |
| K781390 | MYCOPLASMA HYORHINIS (BTS-7) | Flow Laboratories, Inc. | 1978-09-01 | 22 | 0 |
| K771867 | MYCOPLASMA DETECTION KIT | Bioassay Systems Research Corp. | 1977-11-17 | 45 | 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