FRACTURE RISK ASSESSMENT CAPABILITY FOR NORLAND X-RAY BONE DENSITOMETERS— 510(k) K980569

Substantially Equivalent

Norland Corp.

FDA 510(k) clearance K980569 for FRACTURE RISK ASSESSMENT CAPABILITY FOR NORLAND X-RAY BONE DENSITOMETERS, Substantially Equivalent on 1998-06-12. Applicant: Norland Corp..

Clearance details

Applicant: Norland Corp.
Product code: Code KGI
Advisory panel: Radiology
Date received: 1998-02-13
Decision date: 1998-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Atkinson, WI, US

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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.