YOUNG D'GRANULATOR— 510(k) K932255

Name: FDA 510(k) clearance K932255
Creator: U.S. Food and Drug Administration
Published: 1994-04-15

Substantially Equivalent

Young Dental Manufacturing Co. 1, LLC

FDA 510(k) clearance K932255 for YOUNG D'GRANULATOR, Substantially Equivalent on 1994-04-15. Applicant: Young Dental Manufacturing Co. 1, LLC. Device class: 2.

Clearance details

Applicant: Young Dental Manufacturing Co. 1, LLC
Product code: Code KMW
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 1993-05-10
Decision date: 1994-04-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Earth City, MO, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KMW

product code KMW

Injury: 175
Total: 175

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.