510(k) Report

FDA applicant

Cathay Consolidated, Inc.

Taipei, TW2 decisions1985–19970 recalls

FDA records 2 decisions for Cathay Consolidated, Inc. (Taipei, TW) from 1985 to 1997: 2 510(k) clearances. Most are in product codes BYG (Mask, Oxygen) and FNM (Mattress, Air Flotation, Alternating Pressure). 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 Cathay Consolidated, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cathay Consolidated, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cathay Consolidated, Inc.’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

Which product codes does it file in?

  • BYGMask, Oxygen1decision
  • FNMMattress, Air Flotation, Alternating Pressure1decision

What has FDA decided for it lately?

  • K970081Super Air 9000 Alternating Air Floatation Mattress SystemCathay Consolidated, Inc. · 1997
  • K850626Carnation OxygenCathay Consolidated, Inc. · 1985

All 2 as Cathay Consolidated, Inc. →

Other applicant names beginning “Cathay”

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

Cathay Manufacturing Corp. 2Cathay Health Care Equipment Manufacturing, Inc. 1Cathay Manfacturing Corp. 1Cathay International, Ltd. 1