LES RAD FILTER— 510(k) K871227

Name: FDA 510(k) clearance K871227
Creator: U.S. Food and Drug Administration
Published: 1987-06-29

Substantially Equivalent

M. D. Products

FDA 510(k) clearance K871227 for LES RAD FILTER, Substantially Equivalent on 1987-06-29. Applicant: M. D. Products. Device class: 1.

Clearance details

Applicant: M. D. Products
Product code: Code ITY
Device class: Class 1
Regulation: 21 CFR 892.1760
Advisory panel: Radiology
Date received: 1987-03-27
Decision date: 1987-06-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ocala, FL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code ITY

product code ITY

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.