510(k) Report

FDA applicant

Parts Port, Ltd.

Colonial Heights, VA1 decision2000–20000 recalls

FDA records 1 decision for Parts Port, Ltd. (Colonial Heights, VA) in 2000: 1 510(k) clearance. All are in product code 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, cardiovascular panel, where it files most

How often FDA has decided Parts Port, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Parts Port, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Parts Port, Ltd.’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?

  • DXQBlood Pressure Cuff1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K002360Cloud CuffParts Port, Ltd. · 20001cites it

What has FDA decided for it lately?

  • K002360Cloud CuffParts Port, Ltd. · 2000

The one decision as Parts Port, Ltd. →