Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Packard Instrument Co., 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) |
|---|---|---|---|---|---|
| K924907 | FILTERMATE UNIVERSAL HARVESTER | Packard Instrument Co., Inc. | 1992-12-01 | 63 | 0 |
| K913664 | ROSYS MODELS 100 AND 200 | Packard Instrument Co., Inc. | 1991-08-30 | 14 | 0 |
| K901808 | MICROMATE 196 MODEL A961960 | Packard Instrument Co., Inc. | 1990-06-20 | 61 | 0 |
| K883749 | PROBE(TM) MODELS 700 AND 1000 | Packard Instrument Co., Inc. | 1988-11-10 | 70 | 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