Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
General Scanning, 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) |
|---|---|---|---|---|---|
| K980565 | LD2000 SERIES | General Scanning, Inc. | 1998-03-19 | 34 | 0 |
| K973411 | DIGMI-2000 (GSI INTERNAL REFERENCE)/LD2800 (MARKETING NAME) | General Scanning, Inc. | 1997-12-04 | 86 | 0 |
| K923536 | NUCLEAR MEDICINE LASER IMAGER | General Scanning, Inc. | 1992-11-30 | 137 | 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