510(k) Report

FDA applicant

Jason Marine Enterprises, Inc.

Coral Springs, FL1 decision2003–20030 recalls

FDA records 1 decision for Jason Marine Enterprises, Inc. (Coral Springs, FL) in 2003: 1 510(k) clearance. All are in product code ITI (Wheelchair, Powered). 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, physical medicine panel, where it files most

How often FDA has decided Jason Marine Enterprises, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jason Marine Enterprises, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Jason Marine Enterprises, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • ITIWheelchair, Powered1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K031342Jason Marine All Terrain Electric Wheelchair, Model Seeker IIJason Marine Enterprises, Inc. · 20031cites it

What has FDA decided for it lately?

  • K031342Jason Marine All Terrain Electric Wheelchair, Model Seeker IIJason Marine Enterprises, Inc. · 2003

The one decision as Jason Marine Enterprises, Inc. →

Other applicant names beginning “Jason”

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

Jason Marketing Co. 5Jason Co. 1