510(k) Report

FDA applicant

Home Access Health Corp.

Marlborough, MA2 decisions2007–20150 recalls

FDA records 2 decisions for Home Access Health Corp. (Marlborough, MA) from 2007 to 2015: 2 510(k) clearances. Most are in product codes LCP (Assay, Glycosylated Hemoglobin) and JKA (Tubes, Vials, Systems, Serum Separators, Blood…). Its devices cite 5 predicates, 0 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, hematology panel, where it files most

How often FDA has decided Home Access Health Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2007: 12015: 1
2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Home Access Health Corp.’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?

  • LCPAssay, Glycosylated Hemoglobin1decision
  • JKATubes, Vials, Systems, Serum Separators, Blood Collection1decision

Whose devices does it build on?

Its devices cite 5 predicates; 0 are its own earlier devices. The firms it cites most:

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.

  • K141944Home Access Aic TestHome Access Health Corp. · 20152cite it

What has FDA decided for it lately?

  • K141944Home Access Aic TestHome Access Health Corp. · 2015
  • K063852Accessa Cholesterol PanelHome Access Health Corp. · 2007

All 2 as Home Access Health Corp. →