Atlas FDA

Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

National Display Systems · Predicate Candidate Screening

3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K063066AXIS-V MONOCHROME 5 MP DISPLAYNational Display Systems2007-08-033010
K042353AXIS I (1MP), II (2MP), III (3MP), AND V (5MP) MONOCHROME DINational Display Systems2004-11-24860
K040310NOVA FAMILY OF MEDICAL RADIOLOGY DISPLAYSNational Display Systems2004-06-171290

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