BEAMMED SUNLIGHT MINIOMNI BONE SONOMETER— 510(k) K110646

Name: FDA 510(k) clearance K110646
Creator: U.S. Food and Drug Administration
Published: 2011-10-12

Substantially Equivalent

Beam-Med, Ltd.

FDA 510(k) clearance K110646 for BEAMMED SUNLIGHT MINIOMNI BONE SONOMETER, Substantially Equivalent on 2011-10-12. Applicant: Beam-Med, Ltd.. Device class: 2.

Clearance details

Applicant: Beam-Med, Ltd.
Product code: Code MUA
Device class: Class 2
Regulation: 21 CFR 892.1180
Advisory panel: Radiology
Date received: 2011-03-04
Decision date: 2011-10-12
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Petach Tikva, IL

Download summary PDF View on FDA.gov ↗

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