Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Weaver & Co. — 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) |
|---|---|---|---|---|---|
| K885306 | NUPREP | Weaver & Co. | 1989-02-23 | 58 | 0 |
| K883149 | TEN20 CONDUCTIVE | Weaver & Co. | 1988-09-28 | 64 | 0 |
| K874075 | PT-100-30 SOMATOSENSORY STIMULATING ELECTRODE | Weaver & Co. | 1987-10-20 | 14 | 0 |
| K781989 | OMNIPREP | Weaver & Co. | 1978-12-15 | 18 | 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