Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Diagnostic Resources, Inc. · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K914550ANTINUCLEAR ANTIBODY IMMUNOGLOBULIN TEST SYSTEMDiagnostic Resources, Inc.1992-02-111230
K903094STAT TEST HDL/CHOLESTEROL TEST KITDiagnostic Resources, Inc.1990-08-29470
K891050STAT CHEM SYSTEMDiagnostic Resources, Inc.1989-07-201420
K812638DIAGNOSTIC MEDICAL COMPUTERDiagnostic Resources, Inc.1981-11-16620

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