510(k) Report

FDA applicant

Pti

Topeka, KS1 decision1998–19980 recalls

FDA records 1 decision for Pti (Topeka, KS) in 1998: 1 510(k) clearance. All are in product code IMJ (Diathermy, Shortwave, For Use In Applying…). 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 Pti’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pti since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pti 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?

  • IMJDiathermy, Shortwave, For Use In 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.

  • K973732Megapulse IIPti · 19982cite it

What has FDA decided for it lately?

The one decision as Pti →