510(k) Report

FDA applicant

Caird Technology

Columbia, SC3 decisions1998–20110 recalls

FDA records 3 decisions for Caird Technology (Columbia, SC) from 1998 to 2011: 3 510(k) clearances. Most are in product codes DPS (Electrocardiograph) and BZG (Spirometer, Diagnostic). 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 Caird Technology’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2011: 1
2007high 1 (2011) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Caird Technology 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?

  • DPSElectrocardiograph2decisions
  • BZGSpirometer, Diagnostic1decision

Who builds on its devices?

Later devices cite its devices 7 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.

  • K971336Caird Technology SpirometerCaird Technology · 19985cite it
  • K012686Caird Technology Holter 2000Caird Technology · 20012cite it

What has FDA decided for it lately?

  • K101016Ans SystemCaird Technology · 2011
  • K012686Caird Technology Holter 2000Caird Technology · 2001
  • K971336Caird Technology SpirometerCaird Technology · 1998

All 3 as Caird Technology →