Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Teledyne Analytical Instruments — 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) |
|---|---|---|---|---|---|
| K024228 | RX300 OXYGEN ANALYZER | Teledyne Analytical Instruments | 2003-07-17 | 206 | 0 |
| K024155 | MX 300 OXYGEN MONITOR | Teledyne Analytical Instruments | 2003-07-17 | 212 | 0 |
| K001095 | OXYGEN SENSORS, MODELS CIR, C2R, R13, R15, RI7MED, R22MED, R | Teledyne Analytical Instruments | 2000-06-30 | 87 | 1 |
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