Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
PJC · Predicate Candidate Screening
2 FDA 510(k) clearances under this product code; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K121864 | PERKINELMER 226 SAMPLE COLLECTION DEVICES | Perkinelmer, Inc. | 2013-03-12 | 259 | 2 |
| K932661 | WHATMAN BODY FLUID COLLECTION PAPER:WHATMAN BFC180 | Whatman Specialty Products, Inc. | 1996-04-17 | 1050 | 3 |
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