510(k) Report

FDA applicant

Cathaid, Inc.

Miami, FL3 decisions1986–19860 recalls

FDA records 3 decisions for Cathaid, Inc. (Miami, FL) in 1986: 3 510(k) clearances. Most are in product codes KOD (Catheter, Urological) and KGZ (Accessories, Catheter). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Cathaid, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cathaid, Inc.’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?

  • KODCatheter, Urological1decision
  • KGZAccessories, Catheter1decision
  • FGEStents, Drains And Dilators For The Biliary Ducts1decision

What has FDA decided for it lately?

  • K864115Tubegripper, Drainage Catheter & Accessory for SUCathaid, Inc. · 1986
  • K863958Tubegripper, Urological Catheter & AccessoryCathaid, Inc. · 1986
  • K863957Tubegripper, Drainage Catheter & Accessory for GUCathaid, Inc. · 1986

All 3 as Cathaid, Inc. →