510(k) Report

FDA applicant

Paw, LLC

Frederick, MD1 decision2002–20020 recalls

FDA records 1 decision for Paw, LLC (Frederick, MD) in 2002: 1 510(k) clearance. All are in product code ILX (Diathermy, Shortwave, For Use Other Than…). 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 Paw, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Paw, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • ILXDiathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat1decision

Who builds on its devices?

Later devices cite its devices 2 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.

  • K022404ActibandPaw, LLC · 20022cite it

What has FDA decided for it lately?

The one decision as Paw, LLC →