Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Litton Systems, Inc. · 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) |
|---|---|---|---|---|---|
| K013223 | PATIENT VENTILATION OXYGEN CONCENTRATING SYSTEM (PVOCS) | Litton Systems, Inc. | 2002-02-11 | 137 | 0 |
| K951143 | PULSE KLYSTRON AMPLIFIFER (L-5822-90) | Litton Systems, Inc. | 1995-06-19 | 98 | 0 |
| K951142 | PULSE KLYSTRON AMPLIFIER (L-5822-00) | Litton Systems, Inc. | 1995-06-16 | 95 | 0 |
| K873284 | OXYGEN/STERILE AIR GEN SYST/SURGICAL HANDPIECES | Litton Systems, Inc. | 1987-11-16 | 91 | 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