Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
P.K. Morgan , Ltd. — 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) |
|---|---|---|---|---|---|
| K954730 | BENCHMARK TRANSFER TEST | P.K. Morgan , Ltd. | 1997-04-01 | 533 | 0 |
| K960121 | AUTOLINK BODY PLETHYSMOGRAPH | P.K. Morgan , Ltd. | 1997-01-09 | 364 | 0 |
| K954731 | OXYLOG 2 | P.K. Morgan , Ltd. | 1997-01-06 | 448 | 0 |
| K953990 | TRANSFLOW TEST | P.K. Morgan , Ltd. | 1996-12-09 | 473 | 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