Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
GJG · 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) |
|---|---|---|---|---|---|
| K831079 | LIQUIPETTE | The Kendall Company Div. of Tyco Healthcare Group | 1983-04-28 | 24 | 0 |
| K781891 | PIPETTES, PLASTIC DISPOSABLE | Hillwood Corp. | 1978-11-15 | 7 | 0 |
| K780237 | DISPOSABLE CONTROLLED DROP PASTEUR PIPET | Owens-Illinois, Inc. | 1978-03-09 | 24 | 0 |
| K760719 | UNIFORM DROP SIZE PASTEUR TYPE PIPETS | Dade, Baxter Travenol Diagnostics, Inc. | 1976-10-29 | 32 | 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