FDA applicant

Cardiopulmonary Corp.

Milford, CT9 decisions1995–20130 recalls

FDA records 9 decisions for Cardiopulmonary Corp. (Milford, CT) from 1995 to 2013: 9 510(k) clearances. Most are in product codes MSX (System, Network And Communication…) and CBK (Ventilator, Continuous, Facility Use). 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, anesthesiology panel, where it files most

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

FDA decisions per year

1in 2013

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Cardiopulmonary”

FDA records each applicant name separately; these may or may not be the same firm.

Cardiopulmonary Instrumentation 1 Cardiopulmonary Technologies, Inc. 1

Cardiopulmonary Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Cardiopulmonary”