MODIFICATION TO ACCUDEXA BONE DENSITOMETER— 510(k) K001429

Name: FDA 510(k) clearance K001429
Creator: U.S. Food and Drug Administration
Published: 2000-05-26

Substantially Equivalent

Schick Technologies, Inc.

FDA 510(k) clearance K001429 for MODIFICATION TO ACCUDEXA BONE DENSITOMETER, Substantially Equivalent on 2000-05-26. Applicant: Schick Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Schick Technologies, Inc.
Product code: Code KGI
Device class: Class 2
Regulation: 21 CFR 892.1170
Advisory panel: Radiology
Date received: 2000-05-05
Decision date: 2000-05-26
Decision: Substantially Equivalent
Clearance type: Special
Location: Long Island City, NY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KGI

product code KGI

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.