510(k) Report

FDA applicant

Dr. F. Ross Sharp, Ltd.

Canada, CA1 decision1994–19940 recalls

FDA records 1 decision for Dr. F. Ross Sharp, Ltd. (Canada, CA) in 1994: 1 510(k) clearance. All are in product code MEG (Syringe, Antistick). 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, general hospital panel, where it files most

How often FDA has decided Dr. F. Ross Sharp, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dr. F. Ross Sharp, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dr. F. Ross Sharp, Ltd. 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?

  • MEGSyringe, Antistick1decision

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K941450Inviro SyringeDr. F. Ross Sharp, Ltd. · 19943cite it

What has FDA decided for it lately?

  • K941450Inviro SyringeDr. F. Ross Sharp, Ltd. · 1994

The one decision as Dr. F. Ross Sharp, Ltd. →