OSTEOPAK BMD (BONE MINERAL DENSITOMETER)— 510(k) K861515

Name: FDA 510(k) clearance K861515
Creator: U.S. Food and Drug Administration
Published: 1987-02-02

Substantially Equivalent

Siemens Gammasonics, Inc.

FDA 510(k) clearance K861515 for OSTEOPAK BMD (BONE MINERAL DENSITOMETER), Substantially Equivalent on 1987-02-02. Applicant: Siemens Gammasonics, Inc.. Device class: 2.

Clearance details

Applicant: Siemens Gammasonics, Inc.
Product code: Code KGI
Device class: Class 2
Regulation: 21 CFR 892.1170
Advisory panel: Radiology
Date received: 1986-04-23
Decision date: 1987-02-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Des Plaines, IL, 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.