INBODY 770, INBODY 570, INBODY S10, INBODY H20/INBODY H20(B)— 510(k) K123228

Name: FDA 510(k) clearance K123228
Creator: U.S. Food and Drug Administration
Published: 2013-03-08

Substantially Equivalent

Biospace Corporation Limited

FDA 510(k) clearance K123228 for INBODY 770, INBODY 570, INBODY S10, INBODY H20/INBODY H20(B), Substantially Equivalent on 2013-03-08. Applicant: Biospace Corporation Limited. Device class: 2.

Clearance details

Applicant: Biospace Corporation Limited
Product code: Code MNW
Device class: Class 2
Regulation: 21 CFR 870.2770
Advisory panel: Cardiovascular
Date received: 2012-10-15
Decision date: 2013-03-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Naples, FL, 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.