Atlas FDA

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

Jason Marketing Co. — Predicate Candidate Screening

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

59 daysmedian FDA review time
90 days90th percentile
5clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K924133ELECTROTRACE, MODIFICATIONJason Marketing Co.1992-10-30870
K903555ELECTROTRACE DISPOSABLE AG/AGCL EKG MON. ELEC.Jason Marketing Co.1990-11-05900
K896569ELECTROTRACE DISPOSABLE AG/AGCL EKG MONITOR ELEC.Jason Marketing Co.1990-01-18590
K894679ELECTROTRACE DISP. RESTING EKG ELECTRODESJason Marketing Co.1989-09-13500
K871626ELECTROTRACE DISP REST EKG ELECTRODE, CAT. ET1200Jason Marketing Co.1987-06-05390

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