FDA applicant

Pegasus Research Corp.

Costa Mesa, CA12 decisions1988–20120 recalls

FDA records 12 decisions for Pegasus Research Corp. (Costa Mesa, CA) from 1988 to 2012: 12 510(k) clearances. Most are in product codes BTT (Humidifier, Respiratory Gas, (Direct Patient…) and CAF (Nebulizer (Direct Patient Interface)). 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 Pegasus Research Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2007high 1 (2012) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pegasus Research 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 “Pegasus”

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

Pegasus Biologics, Inc. 5 Pegasus Airwave, Inc. 4 Pegasus Medical Supply, Inc. 2 Pegasus Imaging Corp. 1

Pegasus Research 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 “Pegasus”