510(k) Report

FDA applicant

Rudolfo T. Sanchez

Mchenry, IL1 decision1977–19770 recalls

FDA records 1 decision for Rudolfo T. Sanchez (Mchenry, IL) in 1977: 1 510(k) clearance. All are in product code EXE (Protector, Ostomy). 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 Rudolfo T. Sanchez’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rudolfo T. Sanchez since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Rudolfo T. Sanchez 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?

  • EXEProtector, Ostomy1decision

What has FDA decided for it lately?

  • K760927Stoma Shield AdapterRudolfo T. Sanchez · 1977

The one decision as Rudolfo T. Sanchez →