510(k) Report

FDA applicant

Windy Hill Technology, Inc.

Menlo Park, CA2 decisions1999–19990 recalls

FDA records 2 decisions for Windy Hill Technology, Inc. (Menlo Park, CA) in 1999: 2 510(k) clearances. All are in product code KNW (Instrument, Biopsy). 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 Windy Hill Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Windy Hill Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Windy Hill Technology, Inc. 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?

  • KNWInstrument, Biopsy2decisions

What has FDA decided for it lately?

  • K993342Ducprep Breast Aspirator, Model PMPO2Windy Hill Technology, Inc. · 1999
  • K983867Fuji Catheter, Model CTH001Windy Hill Technology, Inc. · 1999

All 2 as Windy Hill Technology, Inc. →