510(k) Report

FDA applicant

Crest Medical Equipment

Mchenry, IL2 decisions1979–19820 recalls

FDA records 2 decisions for Crest Medical Equipment (Mchenry, IL) from 1979 to 1982: 2 510(k) clearances. Most are in product codes KZD (Infusor, Pressure, For I.V. Bags) and DXQ (Blood Pressure Cuff). 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, general hospital panel, where it files most

How often FDA has decided Crest Medical Equipment’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Crest Medical Equipment since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Crest Medical Equipment 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?

  • KZDInfusor, Pressure, For I.V. Bags1decision
  • DXQBlood Pressure Cuff1decision

Who builds on its devices?

Later devices cite its devices 3 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.

  • K790810Disposa-CufCrest Medical Equipment · 19793cite it

What has FDA decided for it lately?

  • K822434Crest Pressure InfusorCrest Medical Equipment · 1982
  • K790810Disposa-CufCrest Medical Equipment · 1979

All 2 as Crest Medical Equipment →