510(k) Report

FDA applicant

Harrison Cbp Seminars

Evanston, WY1 decision2001–20010 recalls

FDA records 1 decision for Harrison Cbp Seminars (Evanston, WY) in 2001: 1 510(k) clearance. All are in product code LXM (Manipulator, Plunger-Like Joint). No recall is linked to its devices.

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

How often FDA has decided Harrison Cbp Seminars’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Harrison Cbp Seminars since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Harrison Cbp Seminars’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?

  • LXMManipulator, Plunger-Like Joint1decision

Who builds on its devices?

Later devices cite its devices 4 times; 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.

  • K010851Harrison Hand Held Adjusting InstrumentHarrison Cbp Seminars · 20014cite it

What has FDA decided for it lately?

  • K010851Harrison Hand Held Adjusting InstrumentHarrison Cbp Seminars · 2001

The one decision as Harrison Cbp Seminars →

Other applicant names beginning “Harrison”

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

Harrison-AI Medical Pty, Ltd. 1