Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Advanced Instrument Development, Inc. — Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
47 daysmedian FDA review time
78 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K974863 | IMIX DIGITAL THORAX SYSTEM | Advanced Instrument Development, Inc. | 1998-03-17 | 78 | 0 |
| K872445 | POWER-AID INDEPENDENT X-RAY POWER SOURCE | Advanced Instrument Development, Inc. | 1987-08-12 | 50 | 0 |
| K827525 | AUTOMATIC EXPOSURE CONTROL TYPE A3300 | Advanced Instrument Development, Inc. | 1982-06-18 | 28 | 0 |
| K813128 | MOBIL-AID AUTOMATIC EXPOSURE CONTROL | Advanced Instrument Development, Inc. | 1981-12-03 | 28 | 0 |
| K791933 | CONVERSION CONTRACTOR TIMER KIT | Advanced Instrument Development, Inc. | 1979-11-13 | 47 | 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