Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Ladd Research Industries, Inc. · Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K893395 | MINI-MONITOR J7000 ICP | Ladd Research Industries, Inc. | 1989-11-22 | 205 | 0 |
| K862820 | LADD/STERITEK ICP MONITOR, CAT. NO. P3000 | Ladd Research Industries, Inc. | 1987-02-26 | 216 | 0 |
| K862012 | LADD MEDICAL S-2000 | Ladd Research Industries, Inc. | 1986-06-09 | 12 | 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