510(k) Report

FDA applicant

Eischoco, Inc.

Gresham, OR2 decisions1997–19990 recalls

FDA records 2 decisions for Eischoco, Inc. (Gresham, OR) from 1997 to 1999: 2 510(k) clearances. All are in product code IRP (Massager, Powered Inflatable Tube). Its devices cite 2 predicates, 1 of them its own earlier devices. 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 Eischoco, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eischoco, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Which product codes does it file in?

  • IRPMassager, Powered Inflatable Tube2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 1 are its own earlier devices. The firms it cites most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K964957Intermittent Compressor SystemEischoco, Inc. · 19971cites it

What has FDA decided for it lately?

  • K991921Intermittent Compression Boot for OtcEischoco, Inc. · 1999
  • K964957Intermittent Compressor SystemEischoco, Inc. · 1997

All 2 as Eischoco, Inc. →