BIA / VITALITY ANALYZER— 510(k) K130856

Substantially Equivalent

Ipgdx, LLC

FDA 510(k) clearance K130856 for BIA / VITALITY ANALYZER, Substantially Equivalent on 2013-11-25. Applicant: Ipgdx, LLC. Device class: 2.

Clearance details

Applicant: Ipgdx, LLC
Product code: Code MNW
Device class: Class 2
Regulation: 21 CFR 870.2770
Advisory panel: Cardiovascular
Date received: 2013-03-28
Decision date: 2013-11-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Littleton, CO, US

Download summary PDF View on FDA.gov ↗

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