FDA applicant

Jason Marketing Co.

Huntington Beach, CA5 decisions1987–19920 recalls

FDA records 5 decisions for Jason Marketing Co. (Huntington Beach, CA) from 1987 to 1992: 5 510(k) clearances. All are in product code DRX (Electrode, Electrocardiograph). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Jason Marketing Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jason Marketing Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Jason Marketing Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Jason”

FDA records each applicant name separately; these may or may not be the same firm.

Jason Co. 1 Jason Marine Enterprises, Inc. 1

Jason Marketing Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Jason”